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Clinical Trials in China / NCT06519617
Enrolling by invitation Phase 2

Study on Optimization and Evaluation of Integrated Chinese and Western Medicine for pSS Glandular Damage

NCT06519617 · tracked via the Priya Life Science China tracker
Sponsor
Qingwen Tao
Phase
Phase 2
Started
2024-07-13
Last updated
2024-07-25

Condition(s) studied

Primary Sjögren Syndrome

Investigational drug(s) / intervention(s)

Yi Qi Yang Yin DecoctionHydroxychloroquine Sulfate

Yi Qi Yang Yin Decoction: The Yi Qi Yang Yin Decoction (Dihuang 15g, Baihe 12g, Nanshashen 15g, celery Qinghao 10g, Malt 10g, Shengma 6g, Chaihu 6g) prescription for patients eligible for qi and yin deficiency was 200 ml twice daily for 12 weeks.

Hydroxychloroquine Sulfate: Hydroxychloroquine Sulfate Tablets 200-400mg daily for 12 weeks.

Study summary

ChatGPT In a randomized controlled trial, 136 patients with primary Sjögren's syndrome (pSS) meeting the inclusion criteria were enrolled and randomly divided into two groups of 68 each. The treatment group received an optimized program combining Chinese and Western medicine for pSS glandular injury, while the control group received a conventional program for pSS glandular damage. The primary efficacy endpoint was the 12-week non-stimulated salivary flow rate (UWS) score. Secondary efficacy endpoints included the glandular damage Visual Analog Scale (VAS) scores, the European Sjögren's Syndrome Patient Reported Index (ESSPRI), among others. The treatment course lasted 12 weeks. The efficacy and safety of the optimized program for pSS glandular injury were evaluated by comparing within and between groups before and after treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * 1\. clinical diagnosis of pSS and qi and yin deficiency ; 2.Sign the informed consent form. Exclusion Criteria: * 1\. pSS activity system damage (ESSDAI score ≥5); 2. Combined connective tissue diseases other than pSS; 3. Pregnant or lactating women; 4. severe cardiovascular and cerebrovascular diseases, liver and kidney failure, and severe malignant tumors; 5. taking psychotropic drugs; 6. assessed by the investigator to be ineligible for enrollment.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
China-Japan friendship hospital Beijing Beijing Municipality

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06519617 on ClinicalTrials.gov ↗ ← All trials in China