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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01463319
Other study ID # ASL07_WW-2011
Secondary ID
Status Completed
Phase Phase 0
First received October 25, 2011
Last updated February 7, 2013
Start date November 2011
Est. completion date September 2012

Study information

Verified date February 2013
Source Presidio Ospedaliero Santa Barbara
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Interventional

Clinical Trial Summary

Unsedated or slightly sedated colonoscopy has fast recovery time, less cost and lower or no incidence of drug-related side effects. May be slightly painful or discomforting for the patient. Based on numerous recent reports, the investigators designed this randomized controlled trial hypothesizing that the use of warm water irrigation versus air insufflation during the insertion phase of colonoscopy might increase the global tolerability of the examination and the proportion of patients undergoing complete colonoscopy without sedation or with a low dose of sedatives.


Recruitment information / eligibility

Status Completed
Enrollment 818
Est. completion date September 2012
Est. primary completion date September 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- 18 Years to 85 Years

- adult patients willing to undergo colonoscopy without routine initial sedation

Exclusion Criteria:

- refuse to initiate colonoscopy without routine sedation

- inadequate bowel preparation

- incapacity to give informed consent

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator)


Related Conditions & MeSH terms


Intervention

Other:
air insufflation
air insufflation during insertion phase colonoscopy
warm water irrigation
warm water irrigation during insertion phase colonoscopy

Locations

Country Name City State
Italy Servizio Endoscopia Digestiva Iglesias Carbonia-Iglesias
Italy U.O.S.D. Diagnostica e Terapia Endoscopica San Gavino Monreale Medio Campidano (VS)

Sponsors (1)

Lead Sponsor Collaborator
Presidio Ospedaliero Santa Barbara

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of patients undergoing complete unsedated or slightly sedated colonoscopy number of patients undergoing complete unsedated conoloscopy with a pain score (as per used scale) =2, or patients with no more than that score AND =2 mg Midazolam E.V. 9 months No
Secondary evaluation of pain and tolerability scores Numeric rating scale, Verbal Descriptor Scale and Faces Pain Scale (0= no pain, 10 worst possible pain.) Hicks CL et al. Pain 2001;93:173-183. Bieri D. et al. Pain. 1990;41(2):138-50. 1 hour No
Secondary percentage of caecum intubation 1 hour No
Secondary time to reach caecum 1 hour No
Secondary Adenoma detection rate Proportion of patients with at least one adenoma of any size 9 months No
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