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Colitis, Ulcerative clinical trials

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NCT ID: NCT02994836 Completed - Ulcerative Colitis Clinical Trials

GIS-SUSANTI-TNF-2015 (Anti-TNF Discontinuation )

Start date: April 21, 2017
Phase: Phase 4
Study type: Interventional

This study will be a multicentre prospective randomized trial to assess the percentage of patients with IBD who, after stopping anti-TNF treatment, have sustained clinical remission at one year compared to those in which the treatment is continued at stable doses

NCT ID: NCT02986724 Completed - Crohn Disease Clinical Trials

A Study to Observe the Safety and Efficacy of Vedolizumab in Biologically Naive Participants With Ulcerative Colitis (UC) or Crohn´s Disease (CD)

CHRONOS
Start date: January 4, 2017
Phase:
Study type: Observational

The purpose of this non-interventional study (NIS) study is to assess further knowledge on the routine use of Entyvio in inflammatory bowel disease therapy, particularly the use in participants with CD and UC naive to biologics.

NCT ID: NCT02985593 Completed - Clinical trials for Healthy Men and Subjects With Ulcerative Colitis

A Phase 1 Study of KHK4083 in Healthy Volunteers and Subjects With Ulcerative Colitis

Start date: December 2016
Phase: Phase 1
Study type: Interventional

The objectives of this study are to evaluate the safety and tolerability of a single intravenous (IV) or subcutaneous (SC) dose of KHK4083 in Japanese or White healthy men in a placebo-controlled, single-blind comparative study, and to evaluate the safety and tolerability of multiple IV doses of KHK4083 in subjects with ulcerative colitis in an open-label study.

NCT ID: NCT02962245 Withdrawn - Ulcerative Colitis Clinical Trials

Efficacy of Treatment With Berberine to Maintain Remission in Ulcerative Colitis

Start date: November 2016
Phase: Phase 4
Study type: Interventional

The research aim to find out whether berberine can reduce the annual recurrence rate of ulcerative colitis in remission. A total of 238 patients with ulcerative colitis in remission will be randomly divided into two groups.One will receive regular treatment,and the other group will receive extra oral berberine 300 mg three times daily for a year. The end of the study for every patient is disease recurrence(Mayo Clinic score of 3 points or more ). The primary analysis is annual recurrence rate, and both endoscopy and Mayo Clinic disease activity index scores at the baseline and final assessments.

NCT ID: NCT02958865 Completed - Ulcerative Colitis Clinical Trials

Study to Compare Oral PF-06651600, PF-06700841 and Placebo in Subjects With Moderate to Severe Ulcerative Colitis

Start date: February 3, 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether PF-06651600 and PF-06700841 are effective in treatment of moderate to severe ulcerative colitis.

NCT ID: NCT02954159 Terminated - Ulcerative Colitis Clinical Trials

Vedolizumab Monotherapy Vs Combination Therapy With Tacrolimus in UC

COVET
Start date: May 18, 2017
Phase: Phase 3
Study type: Interventional

The aim of this study is to assess if a combination therapy of tacrolimus and vedolizumab is superior to vedolizumab monotherapy for induction of remission in moderate to severe UC, and its effect on long and short-term outcomes including colectomy rate. Secondary aim of this study is to assess the safety of tacrolimus as an induction agent in patients with UC.

NCT ID: NCT02943538 Completed - Crohn's Disease Clinical Trials

Telemedicine Crohn's Disease and Ulcerative Colitis (TECCU)

TECCU
Start date: May 2014
Phase: N/A
Study type: Interventional

Pragmatic clinical trial, randomized, controlled parallel, 3 group (group technology platform, call group and control group), developed in the monograph Reference Unit of Inflammatory Bowel Disease Valencia (single-center).

NCT ID: NCT02931799 Not yet recruiting - Crohn Disease Clinical Trials

Prevention of Readmissions at IBD Centres of Excellence

PRICE
Start date: October 1, 2018
Phase: N/A
Study type: Interventional

Patients with Inflammatory Bowel Disease (IBD) are frequently hospitalized, with an increased risk of repeat hospitalizations within the same calendar year. Given that hospital readmissions represent a significant burden to patients and the health care system, a standardised pathway for IBD patients discharged from the hospital can have a significant impact on reducing readmission rates, healthcare utilization and patient satisfaction. The primary aim of this study is to evaluate the effectiveness of an IBD post-discharge pathway, involving post-discharge nurse follow-up and electronic monitoring, in reducing IBD readmission rates.

NCT ID: NCT02931162 Completed - Ulcerative Colitis Clinical Trials

The Effects of Moxibustion on Ulcerative Colitis

Start date: August 23, 2016
Phase: N/A
Study type: Interventional

To investigate the mechanism and effects of moxibustion on patients with ulcerative colitis.

NCT ID: NCT02925260 Completed - Colitis, Ulcerative Clinical Trials

MRI in Normal Ileal Pouches, and a Feasibility Study of Dynamic MRI Enema and Defaecating MRI Pouchography

Start date: May 10, 2017
Phase:
Study type: Observational

A study to investigate the prevalence of pelvic collections in a representative sample of participants with normally functioning ileal pouches. It also aims to establish the feasibility and reporting variables for dynamic MRI enemas in ileal pouches and defaecating enema pouchography.