Clinical trials

18

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Condition / disease
Location
Status: Recruiting

Effect of Single Facial Acupuncture on Dermal Structure and Appearance Satisfaction

This study aims to investigate the effects of a single session of facial rejuvenation acupuncture on skin structure and personal satisfaction with facial appearance. As facial aging involves complex changes in muscles, skin, and soft tissues, facial acupuncture is considered a potential minimally invasive treatment to help restore balance and promote tissue repair. Researchers will enroll 60 healthy adults aged 30 to 60 who are concerned about facial aging. Participants will be randomly assigned to either an immediate intervention group or a waitlist control group. The intervention group will receive one session of facial acupuncture at the start of the study. The control group will continue their normal daily skincare routine for 6 weeks, after which they will receive the same single acupuncture treatment. All participants will be monitored weekly for 6 weeks. The research team will use non-invasive tools, including high-frequency skin ultrasound, 3D facial scanning, and a digital complexion analysis system, to objectively measure changes in skin thickness, facial volume, and wrinkles. Participants will also complete questionnaires at various time points to share their satisfaction with their appearance, self-confidence, and quality of life.

Participants needed: 60
Trial details
Age: 30-60Biological sex: AllType: InterventionalSponsor: Far Eastern Memorial HospitalUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

Adults aged 30 to 60 years old. Individuals concerned about facial aging issues. [+1]

Pregnant women. [+8]

Status: Recruiting

Maternal Methyl-Nutrient Status and Infant Neurodevelopment Study

This prospective cohort study examines the relationship between maternal methyl-nutrient status during pregnancy and offspring neurodevelopment. It integrates maternal dietary, biomarker, genetic, and microbiome data and follows children up to 24 months.

Participants needed: 240
Trial details
Age: 0-45Biological sex: AllType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: May 29, 2026Locations: 2Duration: 2 Years
Eligibility criteria

Aged 20-45 years [+2]

Diagnosed with major chronic diseases, including renal disease (defined as chron... [+5]

Status: Recruiting

Exploring the Feasibility of Transcranial Ultrasound Stimulation in the Treatment of Schizophrenia

1. The purpose of this study is to evaluate the safety and feasibility of transcranial ultrasound stimulation (TUS) treatment in patients with schizophrenia. Subjects are individuals diagnosed with schizophrenia who will receive non-invasive, low-intensity pulsed ultrasound stimulation targeting the hippocampus and its surrounding regions. Evaluations will be conducted before and after the treatment sessions, including electrocardiograms (ECG), blood biochemistry tests, psychiatric symptom assessments, depression level assessments, and cognitive function assessments. 2. The primary objective is to assess the safety of this intervention in patients with schizophrenia. The secondary objective is to explore whether the current stimulation parameters may lead to improvements in the assessed symptoms. Ultimately, this study aims to support the future application of low-intensity pulsed ultrasound as a potential intervention to alleviate symptoms of schizophrenia and improve patients' quality of daily life.

Participants needed: 80
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Far Eastern Memorial HospitalUpdated: Jun 2, 2026Locations: 1
Eligibility criteria

Age: 18-65 years old. [+3]

History of head injury with loss of consciousness for more than 10 minutes or a... [+13]

Status: Recruiting

Exploring Efficacy of Multi-Mode Cognitive Processing Therapy (CPT) for PTSD

This study is a longitudinal, multicenter, single-blind, two-arm randomized controlled trial designed to evaluate the effectiveness of Multi-Modal Cognitive Processing Therapy (MMCPT) for individuals with posttraumatic stress disorder (PTSD). Participants will be randomly assigned to either the intervention group receiving MMCPT or a control group receiving treatment-as-usual (TAU). The intervention follows the standard CPT manual developed by Resick and consists of twelve weekly 90-minute individual sessions. The primary outcomes include PTSD symptom severity assessed by the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) and the PTSD Checklist for DSM-5 (PCL-5). Secondary outcomes include sleep quality (actigraphy, PSQI), anxiety (STAI), depression (HDRS-17), remission rate, and posttraumatic growth (PTGI). Assessments will occur at baseline, mid-treatment, post-treatment, and at 3-, 6-, 9-, and 12-month follow-ups.

Participants needed: 60
Trial details
Age: 20-65Biological sex: AllType: InterventionalSponsor: Far Eastern Memorial HospitalUpdated: Mar 20, 2026Locations: 2
Eligibility criteria

Aged between 20 and 65 years [+4]

Diagnosed with schizophrenia, schizoaffective disorder, or bipolar I disorder [+4]

Status: Not yet recruiting

Effects of Combined Upper Extremity Exercise and Pneumatic Compression Therapy on Breast Cancer-Related Lymphedema

Breast cancer is one of the most common cancers among women worldwide. With advances in treatment, survival rates have steadily increased; however, postoperative complications continue to affect patients' quality of life, with upper extremity lymphedema being among the most prevalent. Breast cancer related lymphedema (BCRL) can result in arm swelling, pain, restricted mobility, and psychological distress, all of which negatively impact daily functioning and social partici pation . Previous studies have demonstrated that regular and moderate upper extremity exercise does not exacerbate lymphedema; instead, it may improve shoulder mobility, muscular strength, and contribute to edema control. In addition, therapeutic modalities such as pneumatic compression pumps and manual lymphatic drainage have been proven effective in reducing swelling and enhancing patient comfort . Recent systema tic reviews further support the beneficial effects of exercise interventions on upper limb function and quality of life in breast cancer survivors. Therefore, combining upper extremity exercise with pneumatic compression therapy may re present a promising integrative intervention to improve lymphedema and related functional limitations. This study aims to investigate the effects of such a combined approach on breast cancer patients with lymphedema by comparing outcomes across multiple ti me points, including arm circumference measurements, shoulder range of motion, upper extremity function (DASH), and quality of life (FACT B), with the goal of establishing a more comprehensive rehabilitation model.

Participants needed: 20
Trial details
Age: 20-70Biological sex: FemaleType: InterventionalSponsor: Far Eastern Memorial HospitalUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

Female breast cancer patients aged 20-70 years [+3]

Breast cancer with a tendency for recurrence or metastasis [+5]

Status: Recruiting

The AIR-CPR Study: AI-Guided Chest Compressions

The AIR-CPR project aims to improve survival rates for patients with Out-of-Hospital Cardiac Arrest (OHCA) by utilizing Artificial Intelligence (AI) to optimize chest compression locations. Current guidelines recommend a standardized compression point (the lower half of the sternum), yet recent research indicates that this position can compress the aortic valve in approximately 48.7% of patients, significantly reducing the chances of successful resuscitation. This study will develop a deep learning model based on YOLO v8 to analyze real-time arterial pressure waveforms to identify proper aortic valve opening and closing. By identifying specific waveform features that humans cannot easily distinguish, the AI will guide rescuers to adjust the compression site-typically toward the left ventricle-to ensure optimal blood output. The project seeks to transform CPR from a standardized "one-size-fits-all" approach into a personalized, precision medicine intervention.

Participants needed: 255
Trial details
Age: 20+Biological sex: AllType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: Feb 24, 2026Locations: 1
Eligibility criteria

Adults aged 20 years or older. [+1]

Pregnant patients. [+8]

Status: Not yet recruiting

The Role of Blood Perfusion in Cervical Cancer, Cervical Intraepithelial Neoplasm and Ovarian Cancer Patients

This study will elucidate the role of 3D transvaginal ultrasound in assessing (1) cervical vascularity and blood flow in patients with cervical cancer and cervical intraepithelial neoplasm, and (2) tumor vascularity and blood flow in patients with ovarian cancer.

Participants needed: 100
Trial details
Biological sex: FemaleType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: Feb 4, 2026Locations: 2Duration: 3 Months
Eligibility criteria

Adult women who have had a normal cervical smear within the past three years and... [+2]

Patients who cannot cooperate with vaginal or abdominal 3D ultrasound scans.

Status: Not yet recruiting

Clinical Outcomes of Non-Indicated Staged Laparotomies in Abdominal Trauma

The goal of this observational study is to understand how often staged operations are performed in abdominal trauma patients without meeting standard clinical criteria, and to explore related clinical characteristics and outcomes. The main questions it aims to answer are: How frequently are staged operations performed when not clinically indicated? What are the clinical features and outcomes of patients who undergo non-indicated staged operations? What are the risk factors for delayed reoperation among patients who initially received a single operation? Researchers will review medical records of patients who underwent exploratory laparotomy for abdominal trauma at Far Eastern Memorial Hospital between January 1, 2013, and December 31, 2024. Participants will be grouped based on whether they had a single or staged operation, and whether their initial operation met established criteria for a staged approach. Clinical characteristics and outcomes will be compared across groups.

Participants needed: 350
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: Aug 7, 2025Locations: 1
Eligibility criteria

This study included patients with abdominal trauma who were admitted to Far East...

Patients who experienced cardiac arrest prior to hospital arrival (OHCA) or in-h... [+2]

Status: Not yet recruiting

The Effect of Nighttime Mirabegron, Solifenacin, Tolterodine, or Oxybutynin on Nocturia, Sexual Function, Autonomic Function, and Lower Urinary Tract Blood Flow Perfusion in Women With Overactive Bladder Syndrome: Randomized Controlled Trial

The optimal medication for women with nocturia remains uncertain. This clinical trial aimed to determine the most effective medication for women with overactive bladder and nocturia. Its primary objectives were to answer the following questions: Which medication is most effective for women with nocturia? Which medication has the least effect on heart rate variability in women with nocturia?

Participants needed: 220
Trial details
Phase: Phase 3Age: 18+Biological sex: FemaleType: InterventionalSponsor: Far Eastern Memorial HospitalUpdated: Aug 11, 2025Locations: 1
Eligibility criteria

>18 years old. [+1]

Clinically significant dysuria (inability to urinate, difficulty urinating). [+3]

Status: Recruiting

The Role of POLE Mutation in High Risk Endometrial Cancer.

The actual role of POLE mutations in high-risk endometrial cancer is undetermined. The main question it aims to answer is: What is the prevalence of POLE mutations in high-risk endometrial cancer case? What is the impact of POLE mutations in real world high-risk endometrial cancer case?

Participants needed: 150
Trial details
Biological sex: FemaleType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: Aug 11, 2025Locations: 1
Eligibility criteria

women with high-risk for recurrent endometrial cancer

Nil

Status: Not yet recruiting

Exploring the Relationship Between Mini-Clinical Evaluation Exercise (Mini-CEX) and Entrustable Professional Activities (EPAs) in Occupational Therapy Clinical Interns' Independent Competence

The goal of this observational cross-sectional study is to evaluate whether the combined use of Mini-Clinical Evaluation Exercise (Mini-CEX) and Entrustable Professional Activities (EPAs) can assess the independent clinical competence of occupational therapy interns at Far Eastern Memorial Hospital. The main questions it aims to answer are: 1. Does the performance on Mini-CEX correlate with the interns' ability to perform independently? 2. Does the use of EPAs provide additional insight into interns' readiness for unsupervised clinical practice? Participants will: 1. Provide informed consent at the sixth week of their internship. 2. Undergo assessment with Mini-CEX and EPAs during their eighth week of clinical training. 3. Complete demographic questionnaires including age, gender, study habits, prior university experience, parental occupation, and residence area.

Participants needed: 50
Trial details
Age: 18-35Biological sex: AllType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: Aug 6, 2025Locations: 1
Eligibility criteria

Occupational therapy interns in the physical domain at Far Eastern Memorial Hosp... [+1]

None specified

Status: Not yet recruiting

Early Speaking Valve in Ventilator Weaning: Effects on Communication, Depression, and Quality of Life

This study evaluates the impact of early tracheostomy speaking valve intervention on communication ability, depression levels, and quality of life in ventilator-dependent patients during the weaning phase. Participants will be randomly assigned to either an experimental group using the Passy-Muir speaking valve or a control group employing standard non-verbal communication methods. Structured questionnaires will be used at multiple time points to assess changes in patient outcomes. The study aims to provide evidence supporting the use of speaking valves to enhance communication and emotional well-being in tracheostomy patients, potentially improving recovery and care strategies.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Far Eastern Memorial HospitalUpdated: Jun 5, 2025
Eligibility criteria

Age: ≥18 years old [+11]

Recent surgery, anesthesia, or sedative use affecting consciousness [+4]

Status: Not yet recruiting

Intraperitoneal Chemotherapy in Recurrent Ovarian Cancer

This study aims to compare intravenous chemotherapy versus intraperitoneal chemotherapy in patients with recurrent ovarian cancer.

Participants needed: 80
Trial details
Age: 20+Biological sex: FemaleType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: Aug 2, 2024Locations: 1
Eligibility criteria

women who had recurrent ovarian cancer and was treated with either intravenous o...

women who did not complete the designated treatment course (exception to those w...

Status: Recruiting

A Multi-center Cardiac PYP Scan Registry in Taiwan

Amyloid deposition in the heart is called cardiac amyloidosis (CA); 95% is immunoglobulin light chain amyloidosis (AL) and transthyretin amyloidosis (ATTR). Hereditary (ATTRm) or wild-type (ATTRwt) depends on whether the ATTRm gene is mutated or not. The most common mutation in Taiwan is A97S, 80% have left ventricular hypertrophy. The good prognosis depends on early diagnosis and correct treatment strategy. Bone-avid tracers such as 99mTc-PYP/DPD/HMDP could detect CA. The mechanism is not clear yet, which may be related to the microcalcification. AL amyloidosis is mostly between visual score grade 0-2, and ATTR-CM is usually grade≥2 on PYP scan, or heart to contralateral (H/CL) ratio, and it might replace invasive myocardial biopsy. However, there are no large-scale clinical studies, lack of standardization data, and limited information in comparison between clinical and imaging parameters. The project will enroll patients with suspected or diagnosed with CA according to CA diagnostic algorithm. Clinical data and image parameters are collected and compared. The project aims to set up prediction models based on the multi-parameters of PYP scan using artificial intelligence technology, including imaging registration and alignment technology, and standardization. The investigators further use the key cardiovascular data elements and imaging-derived database using model training network to extract image features to develop the diagnostic and prognostic prediction models, which are expected to validate the clinical significance and improve patient-centric performance and efficient clinical decision making.

Participants needed: 1,000
Trial details
Age: 20+Biological sex: AllType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: Jul 29, 2024Locations: 1Duration: 1 Year
Eligibility criteria

≥ 20 years of age [+1]

Pregnant or nursing (lactating) women. [+2]

Status: Recruiting

Taiwan Registry of Hypertrophic Cardiomyopathy (THIC) Research Synopsis

Hypertrophic cardiomyopathy (HCM) is hallmarked by the presence of left ventricular hypertrophy (LVH) and may present various symptoms including arrhythmia and heart failure. Mutations in the genes related to sarcomeric proteins and metabolic disorders are known causes of HCM. However, it remains required to further explore the prevalence of HCM in the context of Taiwanese' genetic background. Additionally, certain rare diseases that affect the heart, including Fabry disease, cardiac amyloidosis, may present LVH, which makes precise diagnosis among HCM and these diseases more challenging. In this TSOC multi-center registry, we aim to systematically evaluate the clinical, genetic, biochemical features,prevalence, and possible natural course of HCM and relevant rare diseases such as Fabry disease in Taiwan. In the meanwhile, we may also generate the specific "red-flag" signs of Fabry disease in Taiwan.

Participants needed: 2,600
Trial details
Age: 20+Biological sex: AllType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: Jul 26, 2024Locations: 1
Eligibility criteria

maximal interventricular septal (IVST) and/or posterior wall thickness (PWT) ≥13... [+4]

Patients refuse or unable to give informed consent [+4]

Status: Recruiting

HRT on Overactive Bladder Symptoms, Sexual Function, Depressive Symptoms, Autonomic Function, and Arterial Stiffness

Therefore, the aim of this study is to assess the therapeutic effect on overactive bladder symptoms, sexual function, heart rate variability, arterial stiffness, atherosclerosis, sleep, and depression between tibolone and E2V/MPA. From the results, the investigators will compare the effect of tibolone versus E2V/MPA on overactive bladder symptoms, sexual function, autonomic function, arterial stiffness, atherosclerosis, sleep and depression.

Participants needed: 100
Trial details
Age: 20+Biological sex: FemaleType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: Jun 17, 2024Locations: 1
Eligibility criteria

>20 years old female [+1]

Nil.

Status: Not yet recruiting

Anti-reflux Mucosal Ablation Therapy Randomized Sham Control Trial for Gastroesophageal Reflux Disease

The goal of this randomized clinical trial is to investigate the efficacy and safety of antireflux mucosal ablation (ARMA) for patients with refractory gastroesophageal reflux disease (GERD). The trial aim to evaluate : * Efficacy of ARMA comparing with medical treatment alone (proton pump inhibitor (PPI)), using GERD-Health Related Quality of Life Questionnaire (GERD- HRQL questionnaire), improvement of acid exposure time and DeMeester score * Safety and complications of ARMA Participants will be randomly divided into 2 groups. The intervention group will be undergone ARMA, and the control group will be undergone sham endoscopic treatment. The primary endpoint will be symptoms relief (GERD-HRQL decreases \> 50%). The secondary endpoint will be dosage adjustment of PPI, complications, improvement of acid exposure time and DeMeester score.

Participants needed: 68
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Far Eastern Memorial HospitalUpdated: Feb 23, 2024
Eligibility criteria

Adults aged over 18 years old [+3]

Pregnancy [+13]

Status: Recruiting

The Role of Endometrial Blood Flow in Endometrial Cancer

The incidence of endometrial cancer is gradually increasing nowaday. Sonography can be used to evaluate the endometrial volume, the vascularity and the blood flow. This study will analyze the role of preoperative endometrial blood flow in the outcome of endometrial cancer patients.

Participants needed: 75
Trial details
Age: 20+Biological sex: FemaleType: ObservationalSponsor: Far Eastern Memorial HospitalUpdated: Mar 29, 2023Locations: 1
Eligibility criteria

Not listed