- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07295405
Water Temperature and Bowel Cleansing Quality
Effect of Water Temperature on Bowel Cleansing Quality: A Prospective Observational Study
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Istanbul
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Istanbul, Istanbul, Turkey (Türkiye), 34147
- Bakırköy Dr. Sadi Konuk Training and Research Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria: -Patients aged ≥ 18 years undergoing elective colonoscopy -Ability to provide informed consent -Planned bowel preparation using water-based regimens -No contraindication to warm or cold water intake
Exclusion Criteria: - Emergency colonoscopy -History of inflammatory bowel disease -Prior colorectal surgery -Severe heart failure, renal failure, or electrolyte imbalance -Pregnancy -Inability to complete bowel preparation protocol -Use of additional laxatives outside the study protocol
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
quality of bowel preparation
Time Frame: 01.02.2025-01.07.2025
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The quality of bowel preparation will be assessed using the Boston Bowel Preparation Scale.
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01.02.2025-01.07.2025
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Collaborators and Investigators
Investigators
- Principal Investigator: Nurettin Sahin, MD, Bakırköy Dr. Sadi Konuk Training and Research Hospital
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Bakırkoy Sadi konuk trials
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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