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NCT06309589Completed

The Effectiveness of Combining Ursodeoxycholic Acid With Vitamin D in Treating Patients With Primary Biliary Cholangitis

Department of Infectious Diseases, People's Hospital of Xinjiang Uygur Autonomous Region

Source: ClinicalTrials.gov · Last updated 13 Mar 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this clinical trial is to compare in the effectiveness of combining ursodeoxycholic acid and vitamin D in treating patients with primary biliary cholangitis.

Status (registry)
Completed
Study type
Interventional
Enrollment
60 (actual)
First submitted
1 Mar 2024
Start date
1 May 2021
Primary completion date
30 Sept 2023
Lead sponsor
Yilihamu·Abilitifu
NCT number
NCT06309589

What you commit to

  • Study type: Interventional
  • Participants enrolled: 60
  • From 1 May 2021 to the primary completion date, 30 Sept 2023
  • 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 randomly interrupted or adjusted their medication during the treatment period were excluded.

Other illness

  • The study excluded patients with autoimmune hepatitis or primary sclerosing cholangitis.
  • Patients with other acute and chronic liver diseases were also excluded.
  • Patients with serious cardiopulmonary diseases were excluded as well.

Other

  • Pregnant or lactating women were not included in the study.
  • Patients who lacked follow-up were also excluded.

Who the study is looking for

  • The patient must meet the diagnostic criteria for PBC ;
  • The patient must have been diagnosed at the age of 18 or older;
  • The patient must have completed at least 2 years of treatment and have complete and accessible clinical data;
  • The patient must have strictly followed the doctor's prescription during the treatment period and not have interrupted the treatment arbitrarily.

Age in the registry: 18 years to - · 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
People's Hospital of Xinjiang Uygur Autonomous Region
Coordinator of this site? Confirm its status
ÜrümqiChinaUnknown status

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