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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03187327
Other study ID # 69HCL17_0352
Secondary ID
Status Completed
Phase N/A
First received June 13, 2017
Last updated June 13, 2017
Start date September 2013
Est. completion date January 2015

Study information

Verified date May 2017
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this prospective study, patients who underwent vaginal hysterectomy with salpingectomy or salpingo-oophorectomy were included. The objective of this study is to assess the feasibility of prophylactic salpingectomy during vaginal hysterectomy for benign pathology and the prevalence of occult tubal lesions. The hypothesis is that prophylactic salpingectomy during vaginal hysterectomy for benign pathology present a low failure rate and it makes it possible to avoid the appearance of a certain number of ovarian cancers. The prevalence of bilateral salpingectomy with or without ovariectomy and the prevalence of histopathological and immunohistochemical (p53 expression) abnormalities were evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 69
Est. completion date January 2015
Est. primary completion date November 2014
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients who underwent vaginal hysterectomy for benign pathology with salpingectomy or salpingo-oophorectomy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Hôpital Femme Mère Enfant Bron

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Success rate of the surgical technique prevalence of bilateral salpingectomy with or without ovariectomy Day 0
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