The Biofeedback Therapy in Solitery Rectal Ulser Patients BIOFEEDBACK THERAPY

January 24, 2016 updated by: Serhat Bor, Ege University

The Biofeedback Therapy in Solitery Rectal Ulser Patients

Dissynergic defecation causes solitery rectal ulcer. The biofeedback therapy improves dissynegy and heals soliter rectal ulcer.

Study Overview

Status

Unknown

Conditions

Detailed Description

dyssynergia treating ulcers caused by treatment with biofeedback

Study Type

Observational

Enrollment (Anticipated)

40

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Turkey
      • İzmir, Turkey
        • Recruiting
        • Ege University Faculty of Medicine
        • Principal Investigator:
          • Serhat Bor

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients with solitary rectal ulser

Description

Inclusion Criteria:

  • solitary rectal ulcer in rectosigmoidoscopy
  • type 1 or 3 dissynergic defecation
  • to accept to participate to study and sign informed consent

Exclusion Criteria:

  • previously applied biofeedback
  • serious psychiatric disorder
  • previous anorectal surgery
  • the presence of active malignancy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
ulcer diameter shrinkage
Time Frame: 6-8 weeks
ulcer diameter measured in rectosigmoidoscopy
6-8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Ege University

Investigators

  • Principal Investigator: Serhat Bor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2014

Primary Completion (Anticipated)

January 1, 2017

Study Completion (Anticipated)

January 1, 2017

Study Registration Dates

First Submitted

January 7, 2015

First Submitted That Met QC Criteria

January 7, 2015

First Posted (Estimate)

January 9, 2015

Study Record Updates

Last Update Posted (Estimate)

January 26, 2016

Last Update Submitted That Met QC Criteria

January 24, 2016

Last Verified

January 1, 2016

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • SRUS-BF (Registry Identifier: SRUS-BF)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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