NCT03208283Completed
Evaluation of the Impact of Water Method During Insertion Phase of Flexible Sigmoidoscopy in Training
Evaluation of the Impact of Water Metsertion Phase of Flexible Sigmoidoscopy in the Training of Primary Care Doctors or Nurse Endoscopists for Colorectal Cancer Screening: A Randomized Controlled Study (FSW Study)
Source: ClinicalTrials.gov · Last updated 7 Jul 2026
Brief summary (registry, in English)
Colonoscopy is a sedated procedure traditionally performed using air insufflation during the insertion phase of the procedure. Recently, the use of water method (eg, water infusion or water exchange techniques) during the insertion phase of colonoscopy has been reported to increase the proportion of patients in whom complete unsedated colonoscopy could be achieved, reduce patient recovery time burdens, decrease abdominal discomfort during and after colonoscopy, enhance cecal intubation, and increase willingness to repeat an unsedated colonoscopy. However, there has been no study on the use of water method during the training of primary care doctors or nurse endoscopists in flexible sigmoidoscopy for colorectal cancer screening. In unsedated endoscopic procedure such as FS, endoscope insertion techniques that can potentially reduce patient discomfort and increase the rate of achieving an adequate depth of scope insertion are desirable. Our current study aims to evaluate the impact of water method during insertion phase of FS in the training of primary care doctors or nurse endoscopists for colorectal cancer screening.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 408 (actual)
- First submitted
- 15 May 2017
- Start date
- 28 Oct 2014
- Primary completion date
- 31 Dec 2023
- Lead sponsor
- Chinese University of Hong Kong
- Diseases
- Colorectal cancer
- NCT number
- NCT03208283
What you commit to
- Study type: Interventional
- Participants enrolled: 408
- From 28 Oct 2014 to the primary completion date, 31 Dec 2023
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Personal history of polyposis syndrome, personal history of CRC, personal history of inflammatory bowel disease
Lab values
- Coagulopathy (INR\>1.5) or thrombocytopenia (platelets \<50,000)
Other
- Contraindications for endoscopy due to comorbidities
- Unable to provide written informed consent
- Pregnant patients
Who the study is looking for
- Consecutive asymptomatic patients suitable for CRC screening by FS
- Age 50 - 70 years
- Written informed consent available
Age in the registry: 50 years to 70 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Centre for Digestive Health, Institute of Digestive Disease, Chinese University of Hong Kong Coordinator of this site? Confirm its status | Hong Kong | Hong Kong SAR China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.