Clinical trials

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Status: Not yet recruiting

Machine Learning for Evaluating and Diagnosing Temporomandibular Disorders

This study aims to improve clinical efficiency and effectiveness in treating Temporomandibular Disorders (TMD). The researchers will integrate machine learning technology with clinical examination data, CBCT, and MRI to identify the core underlying issues of each patient. Based on this precise, AI-assisted diagnosis, the study will implement a tailored treatment framework. The final goal is to develop predictive algorithms that can determine MRI necessity while ensuring that clinical interventions are highly targeted, efficient, and successful.

Participants needed: 180
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: En Chu Kong HospitalUpdated: Aug 20, 2026
Eligibility criteria

Patients diagnosed with temporomandibular disorders (TMDs) screened by the Depar... [+3]

Patients meeting any of the following clinical scale thresholds: Generalized Anx... [+10]

Status: Recruiting

Herbal Ointment in Treating Atopic Dermatitis Topically

Atopic dermatitis (AD), also known as atopic eczema, is a chronic inflammatory skin disorder. The current first-line recommended treatment for AD is the use of emollients, topical corticosteroids (TCS), and oral antihistamines if necessary. However, patients often have side effects like skin atrophy and telangiectasia. And there were plenty of herbal medicine which are beneficial to atopic dermatitis in ancient Chinese medicine books and records. Therefore, the purpose of this study is to develop a new topical application of traditional Chinese medicine and evaluate its clinical efficacy in AD patients. In human trial, 66 Subjects diagnosed as AD will be enrolled and treated with Sophora flavescens Aiton topical ointment. After treatment we will estimate the efficacy and record adverse events to conduct statistically analysis. The 1st year project: (1) Expect to enroll 66 clinical subjects of AD. (2) Evaluate subjects 'symptom and proceed herbal ointment treatment. (3) Record treatment responses including adverse effect. (4) Conduct statistically analysis. The 2nd year project: (1) Completing enrollment of 66 clinical subjects of AD. (2) Finish evaluation and treatment of all subjects. (3) Statistically analysis all collecting data (4) Discuss and analyze the outcome.

Participants needed: 66
Trial details
Phase: Phase 2, Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: En Chu Kong HospitalUpdated: Feb 27, 2025Locations: 1
Eligibility criteria

Between 18 and 65 years old, female or male. [+5]

Having a history of topical or systematical hypersensitivity to herbal or its ex... [+5]

Status: Recruiting

Efficacy and Safety of Allium Ureteral Stent for Treating Refractory Ureteral Stricture

To conduct a prospective, multi-center study to observe the long-term efficacy and safety of self expanding ureteral stent for treating participants with refractory ureteral stricture.

Participants needed: 200
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: En Chu Kong HospitalUpdated: Jul 13, 2022Locations: 1
Eligibility criteria

refractory ureteral stricture after at least two times of ureteral dilation

poor cardiovascular function for anesthesia unwilling to accept the long-term pl...