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临床试验/NCT06519617
NCT06519617Enrolling By Invitation2 期

Study on Optimization and Evaluation of Integrated Chinese and Western Medicine for Primary Sjogren's Syndrome Glandular Damage

Qingwen Tao1 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2024年7月13日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
Enrolling By Invitation
发起方
入组人数
136
试验地点
1
主要终点
UWS score

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • clinical diagnosis of pSS and qi and yin deficiency ; 2.Sign the informed consent form.

排除标准

  • pSS activity system damage (ESSDAI score ≥5);
  • Combined connective tissue diseases other than pSS;
  • Pregnant or lactating women;
  • severe cardiovascular and cerebrovascular diseases, liver and kidney failure, and severe malignant tumors;
  • taking psychotropic drugs;
  • assessed by the investigator to be ineligible for enrollment.

研究组 & 干预措施

conventional program group

Sham Comparator

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

干预措施: Hydroxychloroquine Sulfate (Drug)

optimized program combining Chinese and Western medicine for pSS glandular damage

Active Comparator

The herbal prescription for patients eligible for qi and yin deficiency was 200 ml twice daily for 12 weeks.

干预措施: Yi Qi Yang Yin Decoction (Drug)

结局指标

主要结局

UWS score

时间窗: 12 weeks after treatment

unstimulated flow rate of saliva score. it is positive if the UWS ≤1.5 ml/15 min(or 0.1 ml/min). Higher scores(ml/min) mean a better outcome.

次要结局

  • VAS score(12 weeks after treatment)
  • ESSPRI(12 weeks after treatment)
  • Schirmer test(12 weeks after treatment)

研究者

发起方
Qingwen Tao
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Qingwen Tao

chief physician of rheumatism department of Chinese-medicine

China-Japan Friendship Hospital

研究点 (1)

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