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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT01797406
Other study ID # WIC-003
Secondary ID
Status Unknown status
Phase N/A
First received February 20, 2013
Last updated February 21, 2013
Start date February 2013
Est. completion date April 2013

Study information

Verified date February 2013
Source First Affiliated Hospital of Harbin Medical University
Contact Youlin Yang, M.D.
Phone 8613604809322
Email dr.yangylin@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Water injection colonoscopy has been a generally accepted method in training the beginners of colonoscopy for its low pain and less cecal intubation time, the investigators would conduct this study to investigate advantages of this method for experienced endoscopists.


Description:

Up to now, many studies has showed that compared with air insufflation colonoscopy, water-related colonoscopy could shorten the cecal intubation time and relieve the pain of the patients,especially for training the beginners,the effect was notable, but the present researches on water assisted technique has still been confined to following aspects:1.Water infusing was based on air insufflation; predetermined amount of water was infused ,and water was infused while passing through certain segment of the bowel(such as the left half of colon) ; 2.When training the first-learners, certain dose of sedatives or analgesics was injected; 3.The patients recruited were less. Colonoscopies in this study would be performed by experienced endoscopists of air insufflation colonoscopy, water would be injected completely instead of air insufflation while advancing the colonoscope, the amount of the water infused would not be predetermined but vary from individuals, and all the patients would be examined without any sedatives or analgesics.


Recruitment information / eligibility

Status Unknown status
Enrollment 300
Est. completion date April 2013
Est. primary completion date April 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients diagnostic colonoscopy;

- Subjets able to provide informed consent

Exclusion Criteria:

- Prior partial or complete colectomy;

- Patients who decline to participate;

- Patients with poor bowel preparation;

- Contraindications of the colonoscopy

Study Design


Intervention

Other:
Air insufflation
Air is inflated into the bowel to help searching the cavity while advancing the colonoscope until reaching the cecum
Water injection
Water was injected through the working channel instead of air to follow the intestinal cavity until reaching the caecum .

Locations

Country Name City State
China The Gastroenterology Department of the 1st Affiliated Hospital of Harbin Medical University Harbin Heilongjiang

Sponsors (1)

Lead Sponsor Collaborator
First Affiliated Hospital of Harbin Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The success rate of the cecal intubation This will be calculated after the completion of the whole trial,which is about 2 months
Secondary The cecal intubation time(min); This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
Secondary The time to reach the splenic flexure(min) This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
Secondary VAS abdominal pain score Data collected usually within 10minutes post procedure
Secondary The frequency of the colonoscope shortening maneuver while advancing the colonoscope This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
Secondary Length of colonoscope at time of cecal intubation(cm) This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
Secondary Volume of water used during water colonoscopy(ml) This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
Secondary General data of the patients recruited-age Data collected usually within 10minutes post procedure .
Secondary General data of the patients recruited-gender Data collected usually within 10minutes post procedure .
Secondary General data of the patients recruited-BMI Data collected usually within 10minutes post procedure .
Secondary General data of the patients recruited-abdominal or pelvic surgery history Data collected usually within 10minutes post procedure .
Secondary General data of the patients recruited-bowel preparation Data collected usually within 10minutes post procedure .
Secondary The McGill pain evaluation of the abdominal pain Data collected usually within 10minutes post procedure
See also
  Status Clinical Trial Phase
Not yet recruiting NCT02160210 - Ultrafine Endoscope for Colonoscopy in Diagnosis of Colorectal Diseases N/A
Recruiting NCT01797393 - "Air Assisted"Water Injection Colonoscopy in Experienced Endoscopists N/A