ClinConnect ClinConnect Logo
Search / Trial NCT02084186

Moxibustion for Mild and Moderate Ulcerative Colitis

Launched by SHANGHAI INSTITUTE OF ACUPUNCTURE, MOXIBUSTION AND MERIDIAN · Mar 9, 2014

Trial Information

Current as of June 25, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Meet the diagnosis of UC
  • Mayo ≤10
  • Patients should have never received any pharmacological therapy or if they are receiving aminosalicylates and/or prednisolone (the dosage has been taken at least 4 weeks, and should be kept the same as before throughout the trial)
  • Patients should have never received antibiotic, biologicals, probiotics, acetaminophen, acetamide and contraceptive.
  • A written informed consent
  • Exclusion Criteria:
  • Patients with cardiac, encephalic, hepatic, nephric, hematopoietic system, psychotic or any other serious diseases
  • Pregnancy or lactation

About Shanghai Institute Of Acupuncture, Moxibustion And Meridian

The Shanghai Institute of Acupuncture, Moxibustion and Meridian is a leading research organization dedicated to advancing the field of traditional Chinese medicine through rigorous scientific inquiry. With a strong focus on acupuncture and moxibustion techniques, the institute aims to explore and validate the efficacy and mechanisms of these therapies in various clinical settings. Committed to fostering innovation and excellence, the institute collaborates with healthcare professionals and academic institutions to conduct clinical trials and promote evidence-based practices. Through its work, the Shanghai Institute strives to enhance patient care and contribute to the global understanding of integrative medicine.

Locations

Shanghai, , China

Patients applied

0 patients applied

Trial Officials

Huangan Wu, Doctor

Study Director

Shanghai Institute of Acupuncture-Moxibustion and Meridian, Shanghai University of Traditional Chinese Medicine

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials