Ursodeoxycholic Acid in C. Difficile Infection

NCT05526807 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 6

Last updated 2024-04-09

No results posted yet for this study

Summary

The primary objective of the study is to assess tolerability and adherence to treatment with ursodeoxycholic acid

Conditions

  • Clostridioides Difficile Infection

Interventions

DRUG

Ursodeoxycholic acid

Oral

Sponsors & Collaborators

  • Nottingham University Hospitals NHS Trust

    lead OTHER

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-05-08
Primary Completion
2023-12-31
Completion
2023-12-31

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05526807 on ClinicalTrials.gov