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Indeterminate Colitis clinical trials

View clinical trials related to Indeterminate Colitis.

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NCT ID: NCT04672161 Completed - Clinical trials for Ulcerative Colitis (UC)

Education Intervention on Vaccination Adherence Among Inflammatory Bowel Disease (IBD) Patients

Start date: February 4, 2021
Phase: N/A
Study type: Interventional

A retrospective chart review and a six-month prospective outcome analysis aimed to evaluate the efficacy of a vaccination education intervention and vaccination adherence among IBD patients at Weill-Cornell Medical Center. It is hypothesized that a general vaccination education campaign will improve vaccination adherence rates for all IBD patients. Secondarily, it is hypothesized that an Human Papilloma Virus (HPV) vaccination intervention targeted at high-risk IBD patients will increase vaccination adherence among these patients.

NCT ID: NCT03301311 Completed - Ulcerative Colitis Clinical Trials

Personalized Research on Diet in Ulcerative Colitis and Crohn's Disease

PRODUCE
Start date: April 10, 2018
Phase: N/A
Study type: Interventional

A series of N-of-1 trials will be used to determine the effectiveness of a specific carbohydrate diet (SCD) versus a modified SCD in patients in reducing symptoms and inflammatory burden at both the individual and population level. This is a four-year study. The study staff will recruit up to 60 patients across up to 21 sites in patients aged 7-18 with mild to moderate disease activity.

NCT ID: NCT03268213 Completed - Ulcerative Colitis Clinical Trials

Fecal Microbial Transplantation for C. Difficile and/or Ulcerative Colitis or Indeterminate Colitis

FMT
Start date: November 2013
Phase: Early Phase 1
Study type: Interventional

Fecal Microbiota Transplantation will be offered to eligible C. difficile patients (does not require Investigational New Drug designation) and to eligible ulcerative colitis or indeterminate colitis patients as Investigational New Drug treatment

NCT ID: NCT03143517 Completed - Ulcerative Colitis Clinical Trials

Fecal Calprotectin Collection Protocol

CALFE
Start date: April 19, 2017
Phase:
Study type: Observational

The primary objective is to obtain stool samples from subjects diagnosed with , and displaying signs and/or symptoms of IBD and/or IBS will be evaluated in this study. Eligible subjects require a diagnostic colonoscopy with possible biopsy and clinical evaluation.

NCT ID: NCT01966744 Completed - Ulcerative Colitis Clinical Trials

Self-Management Assistance for Recommended Treatment (SMART) Portal

SMART
Start date: July 2013
Phase: N/A
Study type: Observational

The purpose of the study is to develop, evaluate, and optimize an interactive website (the SMART portal). The SMART portal will use IBD-specific and general assessments and interventions to reduce the burden of common barriers to treatment adherence and enhance self-management skills. This study aims to build and revise the SMART portal according to feedback and testing from participants.

NCT ID: NCT01692743 Completed - Ulcerative Colitis Clinical Trials

Telemedicine in Patients With Inflammatory Bowel Disease (TELE-IBD)

TELE-IBD
Start date: September 2012
Phase: Phase 3
Study type: Interventional

Improved methods are needed to monitor patients with inflammatory bowel disease. Telemedicine has shown promise in patients with other chronic diseases; pilot testing in our patients with inflammatory bowel disease demonstrated that the technology was feasible and improved clinical outcomes. The telemedicine system for patients with inflammatory bowel disease (Tele-IBD) should improve outcomes for patients, improve access to care in areas with limited resources, and decrease health care costs.

NCT ID: NCT01536509 Completed - Ulcerative Colitis Clinical Trials

Improving Medication Adherence in Pediatric Inflammatory Bowel Disease

TEAM
Start date: February 2012
Phase: N/A
Study type: Interventional

The purpose of the study is to test an online behavioral intervention to improve medication adherence in children diagnosed with Inflammatory Bowel Disease. Interested families will be monitored for four weeks to determine how frequently their child's IBD medication is taken. Patient's taking less than 90% of medications will be randomized to one of two intervention conditions to complete intervention sessions online. The study consists of 4 online intervention sessions with topics differing by condition and 5 online assessments to complete quality of life questionnaires over a 14 month time frame.