Clinical trials

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

Condition / disease
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Status: Not yet recruiting

A Multicenter Registry-Based Study Across the Spectrum of Degenerative Cervical Myelopathy

This is a multicenter, prospective, longitudinal, observational registry-based study of degenerative cervical myelopathy (DCM) across the full disease spectrum, linked to a disease-specific biobank. The study will enroll adults with non-myelopathic degenerative cervical cord compression, including asymptomatic degenerative cervical cord compression with or without radiculopathy, as well as patients with mild, moderate, or severe DCM. The study does not assign treatment or interfere with real-world clinical decision-making. All participants will undergo standardized baseline assessment, scheduled follow-up, and event-driven supplemental data collection. Core data include demographic information, comorbidities, disease characteristics, neurological examination, objective functional tests, patient-reported outcomes, cervical MRI findings, treatment pathway, treatment changes, adverse events, and long-term clinical outcomes. In participating centers, standardized biospecimen collection will be performed to support nested biomarker, immune, imaging, electrophysiological, and traditional Chinese medicine syndrome substudies. The main objective is to establish a standardized multicenter registry platform covering non-myelopathic degenerative cervical cord compression and mild, moderate, and severe DCM; to describe clinical trajectories, imaging evolution, treatment pathways, and long-term outcomes; and to identify factors associated with disease deterioration and functional prognosis.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Wangjing Hospital, China Academy of Chinese Medical SciencesUpdated: Jun 11, 2026Locations: 1Duration: 36 Months
Eligibility criteria

Age 18 years or older. [+5]

Cervical spinal cord compression or myelopathy mainly caused by non-degenerative... [+3]

Status: Not yet recruiting

Osteoporotic Vertebral Compression Fracture Cohort Study

The study aims to construct an early warning model for Osteoporotic Vertebral Compression Fracture (OVCF) by integrating TCM syndrome patterns with modern risk factors. This is a multi-center cohort study on OVCF integrated with disease and syndrome differentiation in Traditional Chinese Medicine (TCM).

Participants needed: 200
Trial details
Age: 50-80Biological sex: AllType: ObservationalSponsor: Wangjing Hospital, China Academy of Chinese Medical SciencesUpdated: Jan 9, 2026Locations: 4
Eligibility criteria

Patients with serious concomitant cardiovascular/cerebrovascular diseases, liver... [+4]

Status: Not yet recruiting

Huangjing Yangji Formula Combined With Resistance Training for Sarcopenia

The goal of this clinical trial is to learn if a traditional Chinese medicine formula called "Huangjing Yangji Formula," combined with elastic band resistance training, works better than exercise alone to improve physical function and muscle strength in older adults with sarcopenia (age-related muscle loss). The main questions it aims to answer are: Does the combined treatment improve participants' overall physical performance scores more than exercise with a placebo? Does it lead to better outcomes in walking speed, balance, muscle strength, body composition, nutrition, mood, sleep, and overall quality of life? Researchers will compare two groups. One group will take the real Huangjing Yangji Formula granules and do the standardized elastic band resistance training. The other group will take placebo granules (a look-alike mixture with no active medicine) and do the same training. Participants will: Take the assigned granules twice daily for 3 months. Complete a standardized elastic band exercise program 3 times per week for 3 months (with both group and home sessions). Attend three assessment visits (at the start, after 3 months, and 1 month after treatment) for tests and questionnaires. Provide blood samples at the start and after 3 months for routine safety tests and special muscle health markers.

Participants needed: 106
Trial details
Age: 50-75Biological sex: AllType: InterventionalSponsor: Wangjing Hospital, China Academy of Chinese Medical SciencesUpdated: Jan 7, 2026Locations: 3
Eligibility criteria

Aged between 50 and 75 years. [+1]

Secondary sarcopenia due to specific diseases (e.g., active malignancy, hyperthy... [+6]

Status: Not yet recruiting

Clinical Trial of Huoluo Pills Combined With Iguratimod Tablets in the Treatment of Rheumatoid Arthritis

This study aims to systematically evaluate the efficacy and safety of Huoluo Pills combined with Iguratimod Tablets in the treatment of rheumatoid arthritis (RA). A total of 240 patients with RA belonging to the syndromes of Wind - Damp Obstruction or Cold - Damp Obstruction will be enrolled in 8 centers (randomly assigned to groups). The experimental group will receive oral Huoluo Pills combined with Iguratimod Tablets, while the control group will receive oral Iguratimod Tablets alone. Both groups will be administered continuously for 12 weeks. Primary Efficacy Index: The proportion of ACR20 responders in each group at the end of treatment. Key Secondary Efficacy Index: The change in DAS28 (CRP) score from baseline in each group at the end of treatment. Other Secondary Efficacy Indexes: RF, CRP, ESR, IL - 6, ACR50, ACR70, CDAI, SDAI, HAQ - DI, SF - 36, FACIT - Fatigue, and Traditional Chinese Medicine (TCM) syndrome scores. Safety Indexes: Physical examination, blood routine, urine routine, blood biochemistry, coagulation function, etc. This study will investigate the efficacy and safety of Huoluo Pills combined with Iguratimod Tablets in the treatment of RA with Wind - Damp Obstruction or Cold - Damp Obstruction syndromes.

Participants needed: 240
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Wangjing Hospital, China Academy of Chinese Medical SciencesUpdated: Aug 11, 2025
Eligibility criteria

Subjects who meet the Western medicine classification criteria for rheumatoid ar... [+8]

Those who have used plant medicine preparations such as Tripterygium glycosides... [+10]