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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05203978
Other study ID # 2021PI080
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 2022
Est. completion date June 2022

Study information

Verified date February 2022
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Colonoscopy is an exam which can be responsible for pain and discomfort for the patient. Therefore colonoscopy is performed most of the time under general anaesthesia. Moreover, drug-induced sedation comes with adverse effects especially among fragile patients. Besides, monitoring patients during and after sedation is both logistically demanding and costly. Virtual reality offers immersive and three dimensional experiences that distract the attention and might improve patients comfort. The aim of the study is to investigate the use of virtual reality during colonoscopy versus general anaesthesia.


Description:

The study is based on a home made questionnaires completed by the operator and the patient before and after the colonoscopy.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 120
Est. completion date June 2022
Est. primary completion date March 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patient needed planned colonoscopy - able to fill in questionnaires in French Exclusion Criteria: - visual or auditor impairments - dementia patient - limited French language skills - diagnosis of balance disorders or epilepsy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
colonoscopy
Colonoscopy

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Outcome

Type Measure Description Time frame Safety issue
Primary Complete colonoscopy defined by caecum intubation (binary criterion : yes or no) found of the report baseline
Secondary Pain evaluated by Numeric Rating Scale during the procedure (0 no pain and 10 highest imaginable pain) asked on the questionnaire baseline
Secondary Anxiety evaluated by the validated score State Trait Anxiety Inventory ranging from 20 (absence of anxiety) to 80 (highest anxiety) asked on the questionnaire baseline
Secondary Comfort evaluated by Gloucester Comfort Scale between 1 comfortable and 5 severe discomfort asked on the questionnaire baseline
Secondary Satisfaction evaluated on scale of willingness to return (0 no willing at all to 10 definitively willing) asked on the questionnaire baseline
Secondary Polyp removal (binary criterion : yes or no) found on the report baseline
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