Clinical trials

18

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Condition / disease
Location
Status: Not yet recruiting

Effects of Dual Task-Oriented Circuit Training on Walking Recovery in Sub-acute Stroke

This pilot study aims to assess the feasibility, safety, and initial efficacy of an integrated Dual Task-Oriented Circuit Training (DTOCT) program for individuals in the subacute phase of stroke recovery. Although numerous patients recover the capacity to walk in a regulated hospital environment, they frequently encounter difficulties with "community ambulation," the capability to traverse real-world settings while multitasking (e.g., walking while conversing or circumventing barriers). This study will examine if the integration of high-intensity circuit training with cognitive difficulties can promote neuroplasticity and enhance the patient's capacity to safely traverse intricate daily settings.

Participants needed: 36
Trial details
Age: 40-65Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: May 28, 2026Locations: 1
Eligibility criteria

Diagnosed with a first-ever subacute stroke (defined as 2 weeks to 5 months post... [+7]

Expressive or receptive aphasia that impedes task comprehension [+2]

Status: Recruiting

TB Type and Spirometry Result vs. Functional Capacity Based on 6MWT in People With Post-TB Lung Disease

Post-Tuberculosis Lung Disease (PTLD) is defined as chronic respiratory impairment due to previous pulmonary TB. Children recovering from pulmonary TB undergo ongoing respiratory health challenges, including more frequent respiratory symptoms, reduced lung volumes, and a threefold higher rate of pulmonary dysfunction compared to healthy children. These conditions could lead to long-term health consequences such as difficulties in performing daily activities. Pulmonary function impairment in PTLD includes approximately 10% of patients losing more than 50% of lung function. Adolescents who have undergone TB treatment often experience pulmonary function impairment and reduced physical capacity. This aims of this study is to analyze the correlation between type of tuberculosis, spirometry result, and functional capacity in adolescents with post-tuberculosis lung disease. This study is an analytical observational study with a cross-sectional approach. This study is conducted at Department of Physical Medicine and Rehabilitation, Hasan Sadikin Hospital, Bandung, starting in March until May 2026. Inclusion criteria including: adolescents (10-18 year old), and diagnosed with post tuberculosis lung disease by pediatrician, and capable of performing the 6MWT. The participants with post TB lung disease will undergo spirometry and functional capacity assessment using the 6-minute walk test (6MWT). Outcomes include spirometry result and functional capacity using 6MWT.

Participants needed: 20
Trial details
Age: 10-18Biological sex: AllType: ObservationalSponsor: Universitas PadjadjaranUpdated: May 12, 2026Locations: 1
Eligibility criteria

Adolescents (10-18 year old) [+2]

Diagnosed with another lung disease [+1]

Status: Not yet recruiting

Effect of Inspiratory Muscle Training on Diaphragm Function in COPD Patients

This study investigates the effect of threshold inspiratory muscle training on diaphragm thickness and diaphragm excursion, measured using ultrasonography, in patients with stable chronic obstructive pulmonary disease (COPD).

Participants needed: 15
Trial details
Age: 40-59Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Apr 23, 2026
Eligibility criteria

Patients with a COPD GOLD stage 2 [+4]

Patients with contraindications to Inspiratory Muscle Training or spirometry (e.... [+2]

Status: Not yet recruiting

Effect of Immersive Virtual Reality Cognitive Rehabilitation on Subacute Stroke Patients (A Pilot Study)

This pilot randomized controlled trial aims to evaluate the effectiveness of cognitive rehabilitation using an immersive Virtual Reality (VR) system compared to conventional paper-and-pencil cognitive training in subacute stroke patients. A total of 22 participants will be randomly assigned to either the VR intervention group (n=11) or the conventional control group (n=11). The study will measure changes in cognitive function and functional independence

Participants needed: 22
Trial details
Age: 18-59Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Apr 6, 2026Locations: 1
Eligibility criteria

Male or female aged 40-59 years old [+8]

Participants with severe cognitive impairment or aphasia struggle to understand... [+4]

Status: Recruiting

Comparative Effectiveness of Long-Pulsed 1064-nm Nd:YAG and Fractional CO₂ Laser in Skin Rejuvenation

Skin rejuvenation is an effort to improve skin condition from the signs of skin aging. Skin aging is a complex biological process influenced by intrinsic and extrinsic factors, leading to changes in the epidermis and dermis, including decreased collagen characterized by dermal thinning, as well as alterations in skin appearance such as laxity and wrinkles. Laser therapy is one of the treatment modalities for skin rejuvenation, aiming to induce neocollagenesis and collagen remodeling, resulting in dermal thickening and improvement in skin appearance. Fractional CO₂ laser is an ablative laser considered the gold standard therapy for skin rejuvenation, whereas Long Pulsed (LP) Nd:YAG 1064 nm is a nonablative laser that is also used for skin rejuvenation. To date, there have been no studies evaluating the comparative effectiveness between fractional CO₂ laser and LP Nd:YAG 1064 nm for skin rejuvenation. Therefore, research comparing the effectiveness of fractional CO₂ laser and LP Nd:YAG 1064 nm for skin rejuvenation is needed, assessed based on dermal thickness, skin elasticity, wrinkles, and Global Aesthetic Improvement Scale scores.

Participants needed: 15
Trial details
Age: 30-59Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

Male and female patients with skin aging classified as Glogau scale II-III [+1]

Pregnant or breastfeeding women. [+9]

Status: Not yet recruiting

Evaluation and Demonstration of New Tuberculosis Diagnostics for Indonesia

The goal of this cluster-randomised controlled trial (CRCT) is to learn whether the use of new non-sputum-based diagnostic tests and other intervention components for tuberculosis (TB) diagnosis in healthcare facilities (HCF) can increase TB notifications. The main questions it aims to answer are: (1) Does the diagnostic intervention package raise TB notifications by HCF?; (2) Does the diagnostic intervention package raise the proportion of patients with TB who are diagnosed with microbiological tests, lower the time needed for TB diagnosis, lower the number of visits to HCF before TB diagnosis, raise the use of TB tests by healthcare providers, and lower the costs for TB diagnosis? Researchers will compare the diagnostic intervention package provided to HCFs and the community in the intervention arm with the standard of care in the control arm to assess the intervention's effect. Healthcare providers will be trained to provide diagnostic interventions to patients visiting their HCFs and to community residents in the areas surrounding HCFs.

Participants needed: 40,000
Trial details
Age: 29+Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

Cough ≥2 weeks [+11]

Have started TB treatment or TB prophylaxis therapy.

Status: Recruiting

MSC Exosome Therapy for Post-Preeclampsia Endothelial Dysfunction

\--- Why Is This Study Being Done? Women who have preeclampsia during pregnancy face a much higher risk of heart disease later in life. Preeclampsia is a serious pregnancy condition that causes high blood pressure and damages blood vessels. Even after the baby is born, the blood vessels do not fully heal on their own, which can lead to heart problems/cardiovascular years later. This study tests whether a new treatment called exosomes can help repair damaged blood vessels in women who had preeclampsia. Exosomes are tiny particles that come from stem cells and contain healing substances that may help blood vessels work better. \--- What Will Happen in This Study? This study will include 80 women who recently gave birth and had preeclampsia during their pregnancy. Half of the women will receive the exosome treatment through an IV, and half will receive a placebo (a substance with no active treatment). \--- What Will Participants Need to Do? Participants will: * Have blood tests and other health checks * Receive one treatment through an IV * Return for follow-up visits at 1 week after treatment * Have tests to check how well their blood vessels are working Who Can Join This Study? Women who: * Recently gave birth (within 1-2 weeks) * Had preeclampsia during their last pregnancy * Are healthy enough to participate * Can give permission to join the study What Are the Possible Benefits and Risks? The treatment may help repair blood vessel damage and reduce the risk of future heart disease. The exosome treatment appears to be safe based on other studies, but like any medical treatment, there may be side effects. \--- How Long Will the Study Last? The main treatment happens during one visit, with follow-up visits for 1 week to check on participants' health and see if the treatment is working. This research may lead to new ways to protect women's heart health after pregnancy complications.

Participants needed: 80
Trial details
Phase: Phase 1, Phase 2Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Universitas PadjadjaranUpdated: Sep 19, 2025Locations: 1
Eligibility criteria

Postpartum [+3]

History of chronic hypertension prior to pregnancy [+4]

Status: Not yet recruiting

Aerobic and Resistance Training in Post-CABG Patients

This study investigates the effect of combined aerobic and resistance training using resistance bands on diaphragmatic excursion and pulmonary function (FVC, FEV₁, PEF) in post-CABG patients undergoing phase II cardiac rehabilitation.

Participants needed: 15
Trial details
Age: 40-65Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Jun 24, 2025
Eligibility criteria

Patients post-CABG surgery maximum 12 weeks after the procedure [+3]

Blood pressure greater than 160 mmHg for systolic and diastolic blood pressure g... [+2]

Status: Not yet recruiting

0.005% Latanoprost Gel for Nonsegmental Vitiligo

Latanoprost, a prostaglandin F2α (PGF2α) analog used for glaucoma treatment, is known to cause iris darkening, hypertrichosis, and periocular skin hyperpigmentation. PGF2α has been shown to stimulate the growth of melanocyte dendrites, increasing dendricity even at low doses, as well as enhancing tyrosinase activity and quantity, thereby promoting repigmentation. Studies on the use of 0.005% latanoprost gel in both children and adults with vitiligo have demonstrated effective repigmentation without reported side effects.

Participants needed: 10
Trial details
Phase: Phase 2Age: 10-17Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Jun 11, 2025Locations: 1
Eligibility criteria

Patients with non-segmental vitiligo. [+7]

Use of topical therapy (corticosteroids, calcineurin inhibitors, psoralen, and a... [+4]

Status: Not yet recruiting

The Relationship Between Microbioma Balance and Acne Vulgaris as a New Acne Treatment

Background: Acne vulgaris is a chronic inflammatory condition primarily caused by Cutibacterium acnes, which disrupts skin homeostasis, thereby triggering immune responses and sebum metabolism. Dysbiosis is an imbalances in the skin and gut microbiota identified as a significant factor contributing to acne progression. Standard therapy often rely on antibiotics, but the long-term use has increased antibiotic resistance, including in Indonesia. Consequently, alternative methods, such as probiotics and mesenchymal stromal cell (MSC) secretomes are gaining attention for immunomodulatory and regenerative properties. These novel therapies have shown promising results in modulating the skin and gut microbiota while reducing inflammation. Study Design: A phase 2 double-blind randomized controlled trial was adopted using a parallel group design with four arms, namely: (1) standard therapy with oral probiotics and topical secretome (placebo), (2) standard therapy with oral probiotics (placebo) and topical secretome, (3) standard therapy with oral probiotics and topical secretome, and (4) standard therapy with oral probiotics (placebo) and topical secretome (placebo). Sixty-four mild to moderate acne vulgaris patients were randomly allocated to these groups. Interventions were administered over a period of 8 weeks, with outcomes measured at baseline and post-therapy. This study was conducted at Dermatology and Venereology Department of Bali Mandara General Hospital (RSBM). The primary outcome is the reduction of comedones and inflammatory lesions, assessed using the Yolov8 method. Secondary outcomes include gut and skin health parameters, such as tryptophan metabolites, collagen, pH, moisture, sebum levels, and IL-6, to explore the relationship between microbiome balance, skin condition, and inflammation in acne. Discussion: In the context of increasing antibiotic resistance in Indonesia, where therapies often fail to produce sustainable clinical outcomes, this study showed the potential of combining probiotics and MSC secretomes as adjunctive therapies for acne vulgaris. Probiotics restored gut and skin microbiota balance, while MSC secretomes promoted immune modulation and tissue repair. The results of this study paved the way for innovative, non-antibiotic methods for acne management, addressing the need for sustainable and effective therapies amidst growing concerns over dysbiosis and antibiotic resistance.

Participants needed: 64
Trial details
Phase: Phase 2Age: 13-45Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Apr 13, 2025Locations: 1
Eligibility criteria

individuals aged 13 to 45 years [+7]

pregnant patients [+10]

Status: Recruiting

Effect of Modified Poco-Poco Exercise to Frailty Stages, Expression of Global DNA Methylation, GDF15 and Lamin A COP

The goal of this clinical trial is to know the effect of multicomponent exercise in frail elderly in community to aging hallmarks. The main question\[s\] it aims to answer are: 1. Do global DNA methylation levels change in elderly people in Bandung after receiving modified poco-poco exercise? 2. Do GDF15 levels change in elderly people in Bandung after they are given modified poco-poco exercise? 3. Do lamin A COP levels change in elderly people in Bandung after they are given modified poco-poco exercise? 4. Does the level of frailty in elderly people in Bandung change after they are given modified poco-poco exercise? Participants will be asked to do flexibility, balance, aerobic and strengthening exercise included in poco-poco modified exercise three times a week for 12 weeks

Participants needed: 17
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Mar 4, 2025Locations: 1
Eligibility criteria

Frailty level is in pre-frailty [+3]

There is a hearing impairment that may prevent the subject from receiving verbal... [+8]

Status: Recruiting

Recovery Times of Half Dose Sugammadex and Neostigmine for Rocuronium-induced Neuromuscular Blockade

In operating procedure with general anesthesia muscle relaxant is usually used to increase success rate of the operation and to give better outcome. The use of reversal drugs aims to reduce the risk of post-operative complications due to muscle relaxants. Neostigmine is commonly used as a reversal drug, but its indirect mechanism of action results in a long and unpredictable recovery time. Sugammadex directly bind and inactivate rocuronium, in which resulting in a faster and predictable recovery time. However, the high price limits the use of sugammadex. This study aims to compare the effect of half dose sugammadex and neostigmine against the moderate neuromuscular blockade of rocuronium. The main questions it aims to answer are: Does half dose sugammadex gives faster recovery time? Researchers will compare sugammadex to neostigmine to see if sugammadex gives faster recovery time. Participants will: Be given sugammadex or neostigmine as a reversal drug after the operation done

Participants needed: 60
Trial details
Phase: Phase 1, Phase 2Age: 18-59Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Jan 28, 2025Locations: 1
Eligibility criteria

Patients who underwent laparoscopic cholecystectomy under general anesthesia [+3]

History of drug allergies to the agents used [+4]

Status: Recruiting

Safety of Administering Isoniazid to SLE Patients to Prevent TB

Systemic Lupus Erythematosus (SLE) is a prototypical systemic autoimmune disease characterized by heterogeneity, multisystem involvement, and production of multiple autoantibodies. Clinical features can vary, from mild skin and joint involvement to severe and life-threatening conditions. Patients with lupus are more susceptible to infections, in addition to being immunocompromised, and due to the administration of corticosteroid and cytotoxic drugs. The presence of these infections is a cause of death in lupus disease in addition to the activity of the disease itself, especially in Asia-Pacific countries. One infection that often occurs in lupus is Tuberculosis (TB). Efforts have been made to prevent TB infection in vulnerable populations, including isoniazid (INH) prophylaxis. In 2010, World Heatlh Organization issued guidelines for HIV patients to receive INH prophylaxis to prevent TB infection. The implementation of Isoniazid Preventive Therapy (IPT) is quite cheap using INH with mild side effects.18 A meta-analysis study of INH prophylaxis in patients with HIV found that the efficacy of this prophylaxis significantly reduced TB incidence by 35% with an RR of 0.65%. In addition, INH was found to be safe, with no significant increase in drug reactions, according to a meta-analysis of prophylaxis studies in HIV patients. However, there is no guideline for INH prophylaxis for SLE patients, as there is for HIV patients, due to lack of data on this issue. Studies on the effectiveness of INH prophylaxis on the prevention of TB infection for SLE patients should be conducted, but before that, studies on the safety of INH therapy in SLE patients should be conducted.

Participants needed: 60
Trial details
Phase: Phase 2, Phase 3Age: 18-55Biological sex: FemaleType: InterventionalSponsor: Universitas PadjadjaranUpdated: Oct 1, 2024Locations: 1
Eligibility criteria

No signs and symptoms of active TB [+6]

History of allergy to Isoniazid [+3]

Status: Not yet recruiting

Effectivity of Protein Purified Derivative Treatment for Anogenital Warts in HIV Patient

Warts are a common viral infection of the skin and are prevalent throughout the world, with an overall prevalence in the United States estimated at 2-20%. The incidence of anogenital warts occurs more frequently in HIV-infected patients, with a seven-fold increase in risk compared to patients without HIV infection. Available treatments for anogenital warts can only reduce, but cannot eradicate, HPV infection. There are many therapeutic options for treating anogenital warts, but none can prevent recurrence. Immunotherapy has become one of the best therapeutic options for warts caused by HPV infection because it increases the immune response to HPV infection, resulting in remission, both in lesions that receive direct and indirect intralesional therapy. Immunotherapy, acts as a basic principle to enhance cell-mediated immunity for wart clearance. Apart from low recurrence, regression in immunotherapy for warts due to HPV infection generally occurs without cicatrices, so it is a consideration in choosing therapy, including anogenital warts. Various types of immunotherapy have been used, one of which is purified protein derivative, which can be used as an alternative therapy option for anogenital warts. In a previous case report, even though an HIV patient had an abnormal immune system, tuberculin protein purified derivative therapy, immunotherapy provided a significant clinical response in the form of a reduction in lesion size, compared to patients who were not given therapy. Research regarding the comparison of the response to tuberculin protein purified derivative therapy in anogenital warts patients with and without HIV infection has never been reported. Therefore, researchers are interested in examining the comparison of the response to tuberculin purified protein derivative therapy in anogenital warts patients between those with and without HIV infection and knowing the comparison of local and systemic cytokine changes when administering anogenital wart therapy with tuberculin protein purified derivative between those with and without HIV infection.

Participants needed: 30
Trial details
Phase: Phase 2, Phase 3Age: 15-60Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Sep 19, 2024
Eligibility criteria

Anogenital warts whose diagnosis is made based on anamnesis and physical examina... [+1]

1. With a history of allergies to purified protein derivative, generalized derma...

Status: Not yet recruiting

Correlations Between Symptoms of Anxiety And/or Depression with Dysphagia Severity Level

The goal of this observational study is to know any CORRELATIONS BETWEEN SYMPTOMS OF ANXIETY AND / OR DEPRESSION WITH DYSPHAGIA SEVERITY LEVEL in is all of the new or ongoing patients with dysphagia in the Neurorehabilitation Department at Hasan Sadikin General Hospital Bandung and who meet the inclusion and exclusion criteria. The main questions it aims to answer are: Hypothesis 1 H0 : There is no correlation between increased severity of dysphagia and higher levels of anxiety symptoms H1 : There is a correlation between increased severity of dysphagia and higher levels of anxiety Hypothesis 2 H0 : There is no correlation between increased severity level of dysphagia and higher level of depression symptoms H1 : There is a correlation between increased severity of dysphagia and higher levels of depression Hypothesis 3 H0 : There is no correlation between increased severity level of anxiety and dysphagia and higher level of depression symptoms H1 : There is a correlation between increased severity of anxiety and dysphagia and higher levels of depression

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Universitas PadjadjaranUpdated: Sep 19, 2024Locations: 1Duration: 1 Month
Eligibility criteria

Participants aged 18 years and above. [+3]

Participants who have MOCA INA < 18 [+4]

Status: Recruiting

Use of Surface Electromyography as a Tools to Predict Upper Extremity Recovery Function After Stroke

Hypothesis : Based on the framework and premises above, the hypothesis is formulated as follows: H0 : surface electromyography parameters cannot predicts upper extremity motor function recovery in stroke patients H1: surface electromyography parameters can predicts upper extremity motor function recovery in stroke patients

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Universitas PadjadjaranUpdated: Aug 29, 2024Locations: 1Duration: 3 Months
Eligibility criteria

Patients who are hospitalized with upper extremity weakness due to stroke on the... [+2]

Cognitive impairment (MoCA-Ina score less than 26) [+7]

Status: Recruiting

Dexamethasone for Cerebral Toxoplasmosis

Toxoplasma gondii infects over one third of the global human population. Cerebral toxoplasmosis is the most common opportunistic infection in HIV patients resulting in up to 50% of mortality with proper treatment and 80% without it. The fatality mainly due to the brain edema resulted from the mass effect lesion. In addition of anti toxoplasmosis given, adjunctive therapy such as steroid is recommended in order to reduce brain edema, but the dose and duration of administration in cerebral toxoplasmosis has not been evaluated in a clinical trial. Adjunctive therapy given in cerebral toxoplasmosis patients still remains unclear. Moreover, its safety in immunodeficiency cases is still debatable.

Participants needed: 138
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Jul 3, 2024Locations: 1
Eligibility criteria

Age 18 years or above. [+6]

History of anti-toxoplasmosis administrattion for more than 5 days before recrui... [+2]

Status: Recruiting

Effectiveness of ECP Therapy in Stable Angina Pectoris Patients

External Counterpulsation (ECP) is a non-invasive therapy using pressured cuff that is performed on patients with refractory stable angina pectoris to relieve symptoms and increase quality of life. In Indonesia, waiting time for getting coronary artery bypass grafting (CABG) procedure for revascularization treatment in stable angina pectoris patients is way longer than international recommendation which correlates with increase morbidity and mortality during the waiting time. Utilization of ECP for such patients who wait for CABG procedure is still unclear. The investigator aim to evaluate efficacy of addition of ECP compared with medical therapy alone for this population. The efficacy is evaluated using measurement from echocardiography result, treadmill test result, and clinical outcome. if applicable, examination of myocardial perfusion using nuclear examination will also be performed.

Participants needed: 84
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Universitas PadjadjaranUpdated: Sep 25, 2023Locations: 1
Eligibility criteria

Age >= 18 years old [+8]

Congestive Heart Failure [+21]