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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01434927
Other study ID # 07CE2009
Secondary ID
Status Completed
Phase N/A
First received August 18, 2011
Last updated September 13, 2011
Start date October 2009
Est. completion date April 2010

Study information

Verified date September 2011
Source Valduce Hospital
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Observational

Clinical Trial Summary

The study was aimed to prospectively evaluate the acceptance rate of unsedated colonoscopy, in a setting where routine sedation for colonoscopy is standard practice and to characterize the subset of patients willing to try and potentially completing an unsedated procedure.


Description:

Patients were offered to undergo colonoscopy without routine premedication. In case of both acceptance and refusal, a brief questionnaire recording demographics (gender, age, level of education) and clinical features was prospectively recorded in a standard data sheet by one of the four endoscopists at enrollment. Clinical features recorded for each patient included: indication to the procedure, history of abdominal surgery or irritable bowel syndrome, presence of pain as main symptom, chronic use of sedative medications, level of patient's anxiety (none, mild, moderate or severe), main concern about the examination and reason for willing to attempt unsedated procedure.


Recruitment information / eligibility

Status Completed
Enrollment 964
Est. completion date April 2010
Est. primary completion date April 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- adult outpatients

Exclusion Criteria:

1. previous colorectal surgery

2. indication to a bi-directional endoscopy

3. indication to a partial examination

4. patients' refusal or inability to provide informed consent and

5. advanced heart, lung, liver or renal disease (American Society of Anesthesiology risk class III-IV)

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
Unsedated colonoscopy
Patients were offered to undergo colonoscopy without routine premedication
Unsedated colonoscopy
Patients were offered to undergo unsedated procedure. Their demographics and clinical data were recorded

Locations

Country Name City State
Italy Vadluce Hospital Como

Sponsors (1)

Lead Sponsor Collaborator
Valduce Hospital

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary ODDS ratio for unsedated colonoscopy acceptance Multivariate analysis was used to assess the association of dempgraphics (gender, age, level of education) and clinical features (indication to the procedure, history of abdominal surgery or irritable bowel syndrome, presence of pain as main symptom, chronic use of sedative medications, level of patient's anxiety (none, mild, moderate or severe), main concern about the examination and reason for willing to attempt unsedated procedure) to the acceptance of unsedated colonoscopy up to 8 months No
Secondary Acceptance rate of unsedated colonoscopy Proportion of patients accepting to attempt colonoscopy without routine premedication up to 8 months No
Secondary ODDS ratios for unsedated colonoscopy completion Multivariate analysis was used to assess the association of dempgraphics (gender, age, level of education) and clinical features (indication to the procedure, history of abdominal surgery or irritable bowel syndrome, presence of pain as main symptom, chronic use of sedative medications, level of patient's anxiety (none, mild, moderate or severe), main concern about the examination and reason for willing to attempt unsedated procedure) to the completion of unsedated colonoscopy up to 8 months No
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