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NCT07389824Recruiting

Efficacy of Acupuncture-Mesalazine Combination Therapy in Ulcerative Colitis.

Efficacy of Acupuncture Combined With Mesalazine in Inducing and Maintaining Clinical Remission in Mild-to-Moderate Active Ulcerative Colitis: A Single-Center, Randomized Controlled Clinical Trial.

Source: ClinicalTrials.gov · Last updated 25 Aug 2026

Brief summary (registry, in English)

This study aims to evaluate the efficacy and safety of acupuncture combined with mesalazine (an integrated acupuncture-medication regimen) for ulcerative colitis.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
66 (estimated)
First submitted
2 Jan 2026
Start date
1 Feb 2026
Primary completion date
30 Sept 2027
Lead sponsor
Qin Yu
NCT number
NCT07389824

What you commit to

  • Study type: Interventional
  • Planned participants: 66
  • From 1 Feb 2026 to the primary completion date, 30 Sept 2027
  • 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.

Other illness

  • diagnosed with or suspected to have other type of inflammatory bowel disease, such as Crohn's disease;
  • patients in clinical remission or with severe disease activity ( baseline total Mayo score \< 3, or \> 10 );
  • having severe gastrointestinal complications or a recent surgical history, including but not limited to: short bowel syndrome, toxic megacolon, intestinal perforation, complete intestinal obstruction, active massive gastrointestinal hemorrhage, or having undergone major abdominal or intestinal surgery within the past 6 months.
  • significant or unstable comorbidities (e.g., cardiovascular, respiratory, hepatic, or renal diseases);
  • patients with malignant tumors (including but not limited to colorectal cancer);
  • patients with a history of intradermal thumbtack needle embedding;
  • patients with mental illness;
  • patients with either coagulation disorders or skin conditions (such as diseases, infections, ulcers, scars, or tumors at the acupuncture sites) that would preclude acupuncture;
  • any other condition (e.g., geographical remoteness, history of poor adherence) that, in the opinion of the investigator, would make the patient unsuitable for the study or likely to be non-compliant with the protocol.

Other

  • patients unwilling to undergo colonoscopy;
  • pregnant or lactating women;
  • strong needle phobia or unwillingness to receive acupuncture treatment;

Who the study is looking for

  • documented diagnosis of UC;
  • age 18-75 years, regardless of gender;
  • mildly to moderately active UC, defined as a baseline total Mayo score between 3 and 10;
  • willing to receive the complete protocol of intradermal thumbtack needle embedding therapy (12 sessions across three treatment courses);
  • Willing to undergo two colonoscopies (pre-treatment and post-treatment);
  • complete all baseline assessments;
  • capable of understanding and voluntarily sign 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
Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Coordinator of this site? Confirm its status
WuhanChinaRecruiting

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