Evaluating and Treating Potential Research Participants With Digestive Disorders

NCT01736280 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 225

Last updated 2019-11-26

No results posted yet for this study

Summary

Background:

\- Some research studies focus on digestive disorders, such as nutritional, gastrointestinal, and liver disorders. Researchers want to examine and treat people with digestive disorders in order to learn more about these disorders. They also want to study how digestive disorders run in some families. To do so, they will provide standard care to people with digestive disorders. They will also look at relatives of people with digestive disorders, such as parents, children, and siblings.

Objectives:

* To examine and treat people with digestive disorders.
* To evaluate people with digestive disorders for research studies.

Eligibility:

* Individuals of any age who have digestive disorders.
* Individuals at least 2 years of age who are first-degree relatives of the people with digestive disorders.

Design:

* Participants will have at least one outpatient visit to the National Institutes of Health. The visit will last about 2 hours.
* All participants will be screened with a physical exam and medical history. They will also provide different samples for study. Samples may include blood, urine, and stool samples. Saliva and hair samples may also be taken. Skin biopsies and rectal swabs may be collected from adult participants.
* Participants with digestive disorders may be able to receive treatment through this study.

Conditions

Interventions

OTHER

Standard of Care

Any evaluation or treatment under this protocol will be based on standard practice as related to the subjects's digestive disorder.These include but are not limited to biobehavioral interventions including bowel retraining, biofeedback, and other lifestyle interventions, all of which have been shown to be beneficial in the treatment of this type of chronic functional bowel disorder.

Sponsors & Collaborators

  • National Institute of Nursing Research (NINR)

    lead NIH

Principal Investigators

  • Wendy A Henderson, C.R.N.P. · National Institute of Nursing Research (NINR)

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
2 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-09-17
Primary Completion
2019-11-21
Completion
2019-11-21

Countries

  • United States

Study Locations

More Related Trials

Entities

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 NCT01736280 on ClinicalTrials.gov