Clinical trials

12

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Condition / disease
Location
Status: Recruiting

Ultrasound-Guided Extracorporeal Shock Wave Therapy for Calcific Tendinitis

Calcific tendinitis of the shoulder is a debilitating musculoskeletal condition that significantly impacts the working-age population, typically those between 30 and 60 years of age. Accounting for approximately 7- 17% of shoulder pain complaints, it is characterized by the pathological deposition of calcium hydroxyapatite crystals within the rotator cuff tendons, most notably the supraspinatus. The progression of the disease, particularly during the resorptive phase described in Uhthoff's cycle, is associated with a dramatic increase in intratendinous pressure and severe inflammatory pain, leading to substantial functional impairment and socioeconomic burden. While Extracorporeal Shock Wave Therapy (ESWT) is a well established non-invasive modality known to promote calcific resorption via cavitation effects and mechanotransduction-induced neovascularization, its clinical efficacy remains highly variable across current literature, with success rates ranging widely from 47% to 87%. This inconsistency is largely attributed to the limitations inherent in conventional "blind" or landmark-based targeting techniques. Given that calcific deposits are often small, deeply situated, or obscured by the acromion, palpation-guided targeting is frequently unreliable, resulting in suboptimal energy delivery to the pathology and potential collateral damage to surrounding healthy tissues. This one-year research project aims to evaluate the superior efficacy of "Real-time Ultrasound-Guided" ESWT compared to conventional methods. The investigators propose a prospective, randomized, double-blind, controlled trial (RCT) that will recruit 60 patients with confirmed calcific tendinitis. Participants will be stratified by Gärtner classification (Type I-III) to ensure balanced morphological distribution and then randomized into either an experimental group receiving Ultrasound-Guided Focused ESWT or a control group receiving Landmark-based/Sham ESWT. The study incorporates rigorous methodology, including a priori power analysis for sample size estimation, strict allocation concealment, and assessor blinding. Outcomes will be assessed at baseline, 4, and 12 weeks post-treatment. Primary outcomes include the Constant-Murley Score (CMS) and Visual Analog Scale (VAS), while secondary outcomes involve quantitative ultrasound analysis using ImageJ software to measure the reduction in calcific deposit volume and assess tendon integrity. The investigators hypothesize that the integration of realtime ultrasound guidance will significantly enhance therapeutic precision, leading to higher rates of calcific resorption and functional recovery. The findings are expected to provide high-level evidence to standardize ESWT protocols, thereby advancing the implementation of precision medicine in the field of physical and rehabilitation medicine.

Participants needed: 60
Trial details
Age: 20-70Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Aug 12, 2026Locations: 1
Eligibility criteria

Age between 20 and 70 years [+5]

Concomitant full-thickness rotator cuff tear [+7]

Status: Not yet recruiting

Efficacy of an AFCN Proxy Block in Post-TKA Multimodal Pain Management

This randomized controlled trial evaluates the additive effect of Supra-Sartorial Subcutaneous Infiltration (SSSI) when performed in combination with intermittent adductor canal block (iACB) and posterior capsule local infiltration analgesia (PC-LIA) for pain management after total knee arthroplasty (TKA). SSSI, an easy-to-perform tentative proxy block to targeted anterior femoral cutaneous nerve (AFCN) block, is tested in 90 adults (45-90 years) randomized into two arms: active SSSI versus sham SSSI. Primary outcome is pain scores at rest and during movement on postoperative day 0; secondary outcomes include daily pain trajectory at rest and during movement, functional recovery scores, rescue analgesic doses over days 0-3, and quality of recovery assessment on day 4.

Participants needed: 90
Trial details
Age: 45-90Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Adults aged 45-90 undergoing unilateral primary TKA for osteoarthritis. [+3]

Bilateral or revision TKA. [+5]

Status: Recruiting

Effect of the "EMS Back-Up" Ergonomic Program on Paramedics' Manual Handling Safety.

Effect of the "EMS Back-Up" Ergonomic Program on Paramedics' Manual Handling Safety.

Participants needed: 60
Trial details
Age: 20-65Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Mar 30, 2026Locations: 1
Eligibility criteria

Frontline Emergency Medical Technicians (EMTs) or paramedics. [+1]

Non-frontline personnel (administrative only). [+1]

Status: Not yet recruiting

The Effects of Rosuvastatin on Running Training Adaptation and Safety

Statins lower low-density lipoprotein cholesterol (LDL-C) and help prevent atherosclerotic cardiovascular disease, but some users develop statin-associated muscle symptoms (SAMS) such as soreness, stiffness, weakness, or elevated creatine kinase (CK). These symptoms may be more noticeable during exercise. Regular long-distance running improves cardiopulmonary fitness-VO₂max, aerobic threshold (AT), and respiratory compensation point (RCP)-mainly through mitochondrial and metabolic adaptations. Prior studies suggest that lipophilic statins like simvastatin may blunt these adaptations, while hydrophilic statins such as rosuvastatin may have a smaller impact. However, prospective data in habitual endurance runners are limited. This randomized controlled trial will examine how rosuvastatin affects cardiopulmonary fitness improvements and muscle tolerance in individuals who run at least three times per week and meet clinical criteria for statin therapy. After informed consent and baseline cardiopulmonary exercise testing (CPET), participants will be randomized to rosuvastatin 10 mg daily or no statin therapy for three months. Both groups will maintain their usual training routines, and training load will be recorded using heart-rate-based TRIMP. CPET will be repeated monthly to assess changes in VO₂max, AT, and RCP, and muscle enzymes and SAMS will be evaluated at each visit. The study aims to clarify whether rosuvastatin influences endurance-related physiological adaptations or increases muscle symptoms in regular long-distance runners.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years. [+9]

Known allergy or intolerance to statins or rosuvastatin. [+7]

Status: Not yet recruiting

The Effectiveness of Gamified Scenario-based Teaching in Improving Nurses' Awareness and Confidence in Clinical Emergency Care

Research Objective: This study aims to explore the effectiveness of gamified situational teaching in improving nurses' awareness and confidence in clinical emergency response.

Participants needed: 68
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Jan 26, 2026Locations: 3
Eligibility criteria

Not listed

Status: Recruiting

Pelvic Floor Muscle Exercise for Lower Urinary Tract Symptoms After Surgery for Benign Prostatic Hyperplasia.

This study aims to evaluate the effectiveness of pelvic floor muscle exercise (PFME) on improving lower urinary tract symptoms (LUTS), postvoid residual volume (PVR), and quality of life in patients undergoing surgery for benign prostatic hyperplasia (BPH). Patients who undergo BPH-related procedures, such as TURP or HoLEP, often experience postoperative symptoms including urinary urgency, frequency, nocturia, dribbling, and voiding difficulty, which may negatively affect daily living. Pelvic floor muscle exercise is believed to enhance urethral sphincter function and pelvic floor support, thereby improving urinary control. This randomized study assigns participants to either an intervention group receiving PFME training or a control group receiving standard postoperative care. Differences in urinary outcomes between groups will be compared. The findings are expected to provide an accessible and cost-effective rehabilitation strategy to support postoperative recovery and quality of life.

Participants needed: 46
Trial details
Age: 18-99Biological sex: MaleType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Dec 23, 2025Locations: 2
Eligibility criteria

Adults aged 18 years or older. [+2]

Patients with prostate cancer, bladder tumors, or other concomitant urological d... [+2]

Status: Not yet recruiting

Shared Decision-Making for Families in Critical Dialysis Initiation

Background:Acute kidney injury (AKI) is a frequent and serious complication in critically ill patients, often necessitating difficult decisions about starting hemodialysis. While shared decision-making (SDM) is known to improve communication, the effectiveness of structured SDM programs specifically designed for family members in this critical context is not well-established. Aims: The primary purpose of this study is to evaluate the effectiveness of a structured shared decision-making (SDM) program for family members of patients requiring critical hemodialysis initiation. We will assess the program's impact on the quality of the decision-making process (e.g., decision conflict, regret) and the psychological well-being (e.g., anxiety, depression) of the family members. Methods: This study is a parallel-group, randomized controlled trial. Eligible participants (family members of patients with AKI initiating hemodialysis) will be randomly assigned to either an intervention group or a control group. The intervention group will receive a structured SDM support program, while the control group will receive standard care. Primary outcomes, including decision conflict, decision regret, anxiety, and depression, will be measured at baseline and follow-up. Data will be analyzed using the generalized estimating equation (GEE) model to compare the effectiveness between the two groups.

Participants needed: 100
Trial details
Age: 20-99Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Sep 2, 2025
Eligibility criteria

Age ≥ 20 years. [+3]

Age < 20 years.

Status: Recruiting

Prospective Study Between Polysomnography (PSG) and Novel Ultrasonic Jaw Tracking Device in Patients with Sleep Apnea

Obstructive sleep apnea (OSA) affects over 936 million adults worldwide, leading to significant morbidity and reduced quality of life. Traditional diagnostic methods such as polysomnography (PSG), although effective, rely on hospital equipment and human resources and are not widely accessible. Emerging technologies such as the jaw tracking device developed by Sunrise have appeared, using gyroscopes and accelerometers to monitor jaw movements during sleep, showing high diagnostic accuracy compared to PSG. These devices use AI algorithms, providing a practical alternative for OSA diagnosis and monitoring. However, due to the high hardware cost of Sunrise and its rental-based business model, there are logistical challenges and limited monitoring capabilities. This prospective clinical study aims to offer the same capabilities through a novel ultrasonic transmitter for tracking jaw movements during sleep, which can be directly received by using a smartphone microphone, reducing the complexity of setup operations. This study will evaluate the sensitivity of the ultrasonic jaw tracking device in detecting apnea and compare it with PSG standards, developing a deep learning AI-driven algorithm to analyze data from jaw movements, breathing sounds, and apnea-related arousal events, as a basis for continuous home monitoring and evaluation of treatment effects for OSA patients.

Participants needed: 100
Trial details
Age: 20-75Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Mar 6, 2025Locations: 1
Eligibility criteria

Subjects aged between 20 and 75 years. [+4]

Patients currently receiving treatment for sleep apnea (e.g., CPAP therapy or or... [+7]

Status: Recruiting

AI-Driven Cognitive Digital Therapeutics for Dementia Management

The study would investigate the effect of a cognitive digital therapeutics system. The intervention group would receive three digital therapeutics sessions per week for 8 weeks, while the control group would receive usual care. Evaluations would be done at baseline, week 8, and week 16.

Participants needed: 30
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Feb 19, 2025Locations: 1
Eligibility criteria

Age at least 50 years old. [+2]

Mini-mental state examination score below 18 [+6]

Status: Recruiting

Effects of Home-based Surface Electrical Stimulation for Patients with Cervical Myofascial Pain Syndrome

The aim of this study is to compare the developed home-based surface electrical stimulation program to the controls in computer office workers with MPS.

Participants needed: 60
Trial details
Age: 20-60Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Jan 17, 2025Locations: 1
Eligibility criteria

Time of using computer > 4hrs/day [+3]

Had a history of neck surgery [+9]

Status: Not yet recruiting

A Short Regimen for Rifampicin-resistant Isoniazid-susceptible TB

To assess outcome of treatment and safety among patients with rifampicin-resistant isoniazid-susceptible pulmonary tuberculosis treated with a novel regimen consisting of isoniazid, bedaquiline, and moxifloxacin throughout for 6 months, supplemented by pyrazinamide for the initial 2 months.

Participants needed: 100
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Jul 29, 2024
Eligibility criteria

Is willing and able to give informed consent to be enrolled in the trial treatme... [+10]

Is infected with a strain of M. Tuberculosis resistant to isoniazid by Xpert MTB... [+14]

Status: Not yet recruiting

Applying Videos Feedback Learning to Improve Skills Performance of Physiotherapy Interns

This project uses self-practicing videos feedback to learn to improve the skill performance of physiotherapy interns. For traditional physiotherapy intern courses, teachers will conduct core courses and demonstrate teaching, but students are less familiar with the application of skills, even if adding practice course. The learning outcomes of the course are still not good in skill performance. By recording the self-practicing videos, the teacher uses observation and feedback to let the physiotherapy interns know whether the posture of the individual case, the fixed position of the limbs are appropriate, the resistance given and whether the verbal instruction is correct, and based on the evaluation outcomes to observe the students' learning status and clinical thinking ability can improve the skill performance and learning satisfaction.

Participants needed: 90
Trial details
Age: 20-65Biological sex: AllType: InterventionalSponsor: Taipei Medical University WanFang HospitalUpdated: Jun 10, 2024
Eligibility criteria

physical therapy interns require individuals to be over 20 years old.

Individuals unwilling to participate in the study.