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NCT07145060Not yet recruiting

A Study of Yiqi Yangyin Formula in the Treatment of Primary Sjogren's Syndrome

A Randomized Controlled Study of Yiqi Yangyin Formula in the Treatment of Primary Sjogren's Syndrome

Source: ClinicalTrials.gov · Last updated 28 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This project aims to conduct a prospective, randomized, double-blind, controlled clinical study to clarify the efficacy and safety of the YiQi YangYin Formula in treating patients with primary Sjogren's syndrome (pSS) presenting with Qi and Yin deficiency syndrome, with the expectation of providing a scientific basis for the research and development of new traditional Chinese medicine drugs for the effective treatment of pSS.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
105 (estimated)
First submitted
4 Jul 2025
Start date
1 Sept 2025
Primary completion date
31 Jan 2028
Lead sponsor
China-Japan Friendship Hospital
NCT number
NCT07145060

What you commit to

  • Study type: Interventional
  • Planned participants: 105
  • From 1 Sept 2025 to the primary completion date, 31 Jan 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have used cholinergic drugs or artificial tears/saliva in last 1 week;
  • Patients who have participated in or are currently receiving any other experimental drugs or experimental medical devices within the past three months;

Other illness

  • Patients with a history of hypersensitivity or intolerance to any investigational therapeutic drug;
  • Patients diagnosed with secondary Sjogren's syndrome or combined with other connective tissue diseases;
  • Patients with severe lesions in the heart, brain, lungs, liver, kidneys, hematopoietic system, etc., as well as those with malignant tumors or infectious diseases;
  • Other situations that researchers consider ineligible for inclusion (such as cognitive impairment, taking psychotropic drugs).

Other

  • Patients who are pregnant, preparing for pregnancy or breastfeeding;
  • Patients who have used hydroxychloroquine, total glycosides of Paeonia lactide, Iguratimod, cyclophosphamide, cyclosporine A, tacrolimus, and azathioprine in last 1 month;
  • Patients who have used glucocorticoids, methotrexate or mycophenolate mofetil in last 3 months;
  • Patients who have used Leflunomide in last 6 months;
  • Patients who have used rituximab in last 6 months, or have used other biological agents (such as tofacitinib) other than rituximab in last 3 months;

Who the study is looking for

  • Patients aged18-75 years old (including the critical value), gender not limited;
  • Patients meeting the classification criteria of primary Sjogren's syndrome in ACR/EULAR 2016;
  • Patients with dry mouth VAS ≥4 and ESSDAI score \< 5;
  • Patients with positive autoantibodies (ANA or anti-SSA antibodies or anti-SSB antibodies or RF) and/or hyperimmunoglobulinemia or increased erythrocyte sedimentation rate;
  • Patients meeting the syndrome of qi and Yin deficiency in traditional Chinese medicine;
  • The subjects were informed and voluntarily signed the informed consent form.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
China-Japan Friendship Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.