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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03157752
Other study ID # RECHMPL17_0145
Secondary ID
Status Completed
Phase N/A
First received May 15, 2017
Last updated December 1, 2017
Start date May 31, 2017
Est. completion date September 30, 2017

Study information

Verified date May 2017
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In France, screening involves a routine test of papanicolaou in women aged 25 to 65 years. In the case of an abnormal Pap smear discovery, the diagnostic strategy is based in most cases in colscopy to allow cervical biopsies if necessary to obtain a histological diagnosis of high quality cervical intraepithelial neoplasia (CIN) (2- 3) which, if persistent, can cause cervical cancer. Their results, also in the case of the persistence of a low-level lesion or of a cyto-histological discordance, indicate conization. Conization is a procedure performed by resection of the diathermic grip, allowing a simple and fast gesture compatible with a load under local anesthesia. In order to simplify the overall cost of the patient, more and more conizations of Montpellier and Nimes take place under local anesthesia. .

The main objective of our study is to evaluate the overall satisfaction of patients in the case of conisation under local anesthesia.

The goal is to promote local anesthesia for the management of congested patients, which simplifies overall management, reduces cost and reduces complications associated with general anesthesia.


Description:

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Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Quality of life questionnaire
Quality of life questionnaire

Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Montpellier Centre Hospitalier Universitaire de Nimes

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient satisfactio Overall satisfaction of the patient, evaluated by the completion of a questionnaire on the day of the intervention. 1 day
See also
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