Clinical trials

12

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effectiveness of Neuroplasticity-Targeted Supplements on Neuroinflammatory Markers, ADHD Symptom Severity, and Clinical Scores in Children

This randomized controlled trial will evaluate the effectiveness of neuroplasticity-targeted supplements on neuroinflammatory markers and ADHD symptoms in children aged 6 to 12 years diagnosed with Attention Deficit Hyperactivity Disorder (ADHD). Participants will be randomly assigned to one of four groups: gut-targeted supplements (prebiotics and probiotics), brain-targeted supplements (omega-3 fatty acids and vitamin B1), combined supplementation, or placebo. The intervention period will last 12 weeks. Primary outcomes include changes in ADHD symptom severity and clinical scores using validated rating scales. Secondary outcomes include changes in biomarkers of neuroinflammation and neuroplasticity, including IL-6, TNF-alpha, BDNF, short-chain fatty acids, and Claudin-5.

Participants needed: 68
Trial details
Age: 6-12Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

DSM-5 confirmed ADHD diagnosis [+2]

Antibiotic use in last 4 weeks [+3]

Status: Recruiting

Efficacy of Combining Mulligan Spinal Mobilization With Leg Movement and Mechanical Lumbar Traction in Lumbar Radiculopathy

Lumbar radiculopathy (LR), often caused by disc herniation, results in significant pain, disability, and reduced quality of life. Spinal Mobilization with Leg Movement (SMWLM) is a manual technique that has shown promise, while mechanical lumbar traction is used to reduce nerve compression, though its standalone effectiveness is debated. This randomized controlled trial aims to compare the combined effect of SMWLM plus mechanical lumbar traction against SMWLM alone, both administered with conventional physiotherapy. Outcomes will be assessed over 4 weeks to determine if the combined intervention offers superior pain relief, functional improvement, and range of motion in patients with unilateral L4-L5 or L5-S1 radiculopathy.

Participants needed: 32
Trial details
Age: 20-50Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: May 7, 2026Locations: 1
Eligibility criteria

Age 20-50 years [+5]

Cognitive impairment, dementia, central cord signs [+5]

Status: Recruiting

Comparison of Radiological Outcome of Conventional vs Accelerated Ponseti Casting Technique for Treatment of Club Foot

Club foot (congenital talipes equinovarus) is a common birth deformity affecting 1-2 per 1,000 live births, with even higher rates in low-income countries. The standard treatment is the Ponseti method using weekly serial casts, but weekly visits for several weeks can be challenging for families in hot climates or with limited resources. This randomized controlled trial compares the standard once-weekly Ponseti casting with an accelerated twice-weekly casting technique. The primary outcome is radiological correction measured by the lateral talocalcaneal angle (target ≥35°) on standardized foot X-rays taken six weeks after brace fitting. Secondary outcomes include the talocalcaneal index (\>40) and the tibio-calcaneal (dorsiflexion) angle (60-90°). Babies under six months of age with idiopathic club foot will be randomly assigned to either the standard or accelerated casting group. All other aspects of the Ponseti method (manipulation, number of casts, tenotomy when needed, final cast for three weeks, and foot abduction orthosis) remain identical. Adverse events such as skin problems, swelling, or cast complications will be recorded. The study aims to determine whether accelerated casting achieves better radiographic correction without increasing risks.

Participants needed: 144
Trial details
Age: 1-5Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Apr 28, 2026Locations: 1
Eligibility criteria

Syndromic club foot (e.g., associated with arthrogryposis, myelomeningocele, or... [+2]

Status: Recruiting

Impact of Chewing Gum on Postoperative Gut Motility in Gastrointestinal Surgery Patients

Postoperative ileus (POI) is a frequent complication after abdominal surgery, leading to delayed gastrointestinal motility, prolonged hospital stay, and increased patient discomfort. Chewing gum, as a form of sham feeding, has been proposed to stimulate gut motility through vagal stimulation and increased gastrointestinal secretions. This randomized controlled trial aims to assess the effect of chewing gum on early recovery of gastrointestinal motility in patients undergoing open gastrointestinal surgery.

Participants needed: 96
Trial details
Age: 17-85Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Age between 17 and 85 years. [+3]

Patients with metabolic or endocrine disorders (diabetes mellitus, hypothyroidis... [+5]

Status: Recruiting

Integrated Oral Care Intervention for Xerostomia in Diabetes Patients

Diabetes patients commonly experience dry mouth also known as xerostomia which can affect eating speaking oral health and overall quality of life. This study evaluates whether simple oral care actions delivered by endocrinologists during routine diabetes clinic visits can improve dry mouth symptoms and oral health related quality of life. Endocrinologists will be trained to screen for dry mouth provide brief counseling prescribe saliva substitutes and refer patients to dental services when needed. Adult patients with diabetes and symptoms of dry mouth will be followed before and after the intervention to assess changes in xerostomia severity and oral health outcomes. The study will also explore barriers and facilitators to integrating oral health care into routine diabetes management in Pakistan.

Participants needed: 80
Trial details
Age: Up to 18Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Presence of a single stone in the renal pelvis. [+3]

Patients with multiple kidney stones. [+3]

Status: Recruiting

Comparative Study of Functional Outcomes Between Peroneus Longus and Hamstring Tendon Autografts in Arthroscopic ACL Reconstruction

This is a prospective, single-blinded, randomized controlled trial. Sixty patients (≥18 years) with an isolated ACL injury will be randomly assigned to receive an ACL reconstruction using either a Peroneus Longus Tendon (PLT) autograft or a Hamstring Tendon (HST) autograft. The primary objective is to compare early functional outcomes between the two groups at 6 weeks and 3 months post-surgery, using the Lysholm Knee Score. The study aims to demonstrate the non-inferiority of the PLT graft. All surgeries will be performed arthroscopically at Khyber Teaching Hospital, Peshawar, followed by a standardized rehabilitation protocol.

Participants needed: 64
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Jan 16, 2026Locations: 1
Eligibility criteria

Patients aged 18 years or older. [+2]

Multiligament knee injuries (e.g., concomitant PCL, MCL, or LCL injuries). [+3]

Status: Recruiting

Impact of Diet and Nutrition on Growth and Development in Young Children

The association between nutrition in early life and its long-term health consequences has long been known. However, there is a scarcity of scientific evidence on how nutritional status affects child growth and development in remote, rural agro-pastoral communities with distinct dietary intake habits, geographical location, socio-economic status, and cultures.

Participants needed: 832
Trial details
Age: 1-24Biological sex: AllType: ObservationalSponsor: Khyber Medical University PeshawarUpdated: Jan 8, 2026Locations: 1
Eligibility criteria

Households living in the area from the last two 2 years. [+2]

Children with any co-existent systemic diseases, confirmed from medical records. [+2]

Status: Recruiting

Effect of Conventional vs Intensive Management on Gestational Diabetes and Maternal Fetal Outcomes

This study involved two management protocols to manage diabetes in pregnancy. Sixty patients having GDM will be recruited on the basis of the OGTT and randomly allocated to two management groups. One group of patients will receive counselling and the conventional method of management. while the other group will receive a tailored diet plan and physical activity with low caloric and moderate intense exercises. Both groups will receive a dietary plan based on their sugar levels weekly basis and physical activity with pharmacotherapy to adjust their sugar levels, while the intensive group will have rigorous monitoring on a monthly basis and frequent visits with repeated lab checks. This will help us to reduce short and long-term complications with improved maternal and neonatal outcomes.

Participants needed: 60
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Jan 13, 2026Locations: 2
Eligibility criteria

Maternal age between 18-45 years [+2]

Patients having twin pregnancies [+5]

Status: Recruiting

Impact of Lifestyle Interventions on Cognitive Decline in Non-alcoholic Fatty Liver Disease

This study investigates whether a structured lifestyle program can help improve thinking skills and liver health in adults with Non-Alcoholic Fatty Liver Disease (NAFLD). We are enrolling 45 participants, aged 18-42, who will be randomly assigned to one of three groups for six months: one receiving general health advice, a second following a supervised Mediterranean diet plan, and a third combining the same diet with a regular walking program. The main goal is to see if these diet and exercise interventions can lead to better scores on memory and reasoning tests, reduce liver stiffness measured by a painless scan (FibroScan), and improve related blood markers of inflammation and hormone balance.

Participants needed: 45
Trial details
Age: 18-42Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Dec 19, 2025Locations: 2
Eligibility criteria

Age 18 to 42 years. [+3]

History of alcohol intake >20g/day. [+4]

Status: Recruiting

Comparison Of Clinical Effects Of Listerine And Chlorhexidine Mouth Wash In Patients Undergoing Fixed Orthodontic Treatment

This randomized clinical trial aims to compare the effectiveness of Listerine and Chlorhexidine mouthwashes in improving periodontal health in patients undergoing fixed orthodontic treatment. Gingival Index and Plaque Index will be assessed at baseline, 2 weeks, and 4 weeks.

Participants needed: 60
Trial details
Age: 13-40Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Nov 26, 2025Locations: 1
Eligibility criteria

Aged 13-40 years [+2]

Systemic illness (e.g., diabetes, heart disease, hepatitis) [+5]

Status: Recruiting

Bone Turnover Markers and Treatment Efficacy in Postmenopausal Osteoporosis

This study investigates the use of blood tests known as Bone Turnover Markers (BTMs) to quickly monitor the effectiveness of osteoporosis treatment in postmenopausal women. Osteoporosis, which weakens bones and increases fracture risk, is typically monitored using a DEXA scan to measure bone density (BMD), but this method changes slowly. BTMs may show a response to medication within just 3 to 6 months. In this randomized controlled trial, 40 postmenopausal women with osteoporosis will be assigned to receive either antiresorptive drugs (which slow bone loss) or anabolic drugs (which build new bone), along with calcium and vitamin D. The study will compare how these treatments affect BTMs and BMD over six months to determine if BTMs can serve as an early and reliable indicator of treatment success, which could be particularly useful in regions like Pakistan where access to repeated DEXA scans is limited.

Participants needed: 40
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Nov 21, 2025Locations: 1
Eligibility criteria

Postmenopausal women (at least one year since last menstrual cycle). [+5]

Women with multiple vertebral fractures or severe lumbar degenerative changes. [+4]

Status: Recruiting

Engagement of coMmunity Through Participatory Learning and Action for cOntrol and preVEntion of Type II Diabetes and Its Risk Factors [EMPOWER-D]

This project aims to adapt, implement, and evaluate Participatory Learning and Action (PLA) based intervention in rural areas of KPK, Pakistan which includes Peshawar and Swabi for TIIDM prevention and control. The pivotal components of this approach include adapting, implementing, and evaluating the PLA-based intervention for the prevention and control of Type II diabetes. These components will be tailored to meet the specific needs of two different settings in Peshawar and Swabi, Pakistan. Type II Diabetes Mellitus (TIIDM) is considered the fastest-growing health emergency, affecting 537 million adults worldwide. Global projections for the year 2045 suggest that a 12.2% rise in TIIDM is anticipated with an additional 11.4% rise for intermediate hyperglycemia (IHG) \[1\]. Around 80% of people with TIIDM reside in low-and middle-income countries (LMICs), exhausting the already burdened healthcare system \[2\]. The intervention "Community groups or mobile phone messaging to prevent and control type 2 diabetes and intermediate hyperglycemia in Bangladesh (DMagic)" has been tested and found effective in the rural context of Bangladesh \[1-3\]. A full trial will be conducted in the rural areas of Peshawar and Swabi, Pakistan. It is anticipated that with the use of evidence-based approaches, best practices, and meaningful community participation, PLA is expected to enhance social and behavioural determinants of health and subsequent outcomes. This will further pave the way for the control of other NCDs through a similar focused approach.

Participants needed: 12,744
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Sep 2, 2025Locations: 1
Eligibility criteria

Individuals aged 20 years and above. [+4]

Individuals below the age of 20 years. [+3]