Satisfaction and Long-term Anatomic Efficacy Study on Patients Who Underwent a Richter Intervention in the Obstetric and Gynecology Department of Foch Hospital Since 2008

NCT ID: NCT03901586

Last Updated: 2019-05-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

88 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-12-01

Study Completion Date

2019-04-30

Brief Summary

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Satisfaction and Long-term Anatomic Efficacy will be assessed on Patients Who Underwent a Richter Intervention in the Obstetric and Gynecology Department of Foch Hospital Since 2008.

Detailed Description

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Satisfaction and Long-term Anatomic Efficacy will be assessed on Patients Who Underwent a Richter Intervention in the Obstetric and Gynecology Department of Foch Hospital Since 2008.

Conditions

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Genital Prolapse

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Patients who had Richter intervention

Group Type EXPERIMENTAL

Satisfaction assessment

Intervention Type OTHER

Patient will be asked to assess their satisfaction concerning the Richter procedure and its long term effect

Quality of life

Intervention Type OTHER

The Quality of life will be assessed with 3 questionnaires (I-Qol / PISQ-12/PFDI-20)

Gynecological assessment

Intervention Type OTHER

An optional gynecological consult is proposed to the patients to better estimate the gynecological long-term impact of the procedure

Interventions

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Satisfaction assessment

Patient will be asked to assess their satisfaction concerning the Richter procedure and its long term effect

Intervention Type OTHER

Quality of life

The Quality of life will be assessed with 3 questionnaires (I-Qol / PISQ-12/PFDI-20)

Intervention Type OTHER

Gynecological assessment

An optional gynecological consult is proposed to the patients to better estimate the gynecological long-term impact of the procedure

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient who underwent a Richter intervention between 01/01/2008 and 31/12/2017 in the Gynecology Department of Foch Hospital

Exclusion Criteria

* None
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Hopital Foch

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Angeline Favre-Inhofer

Role: PRINCIPAL_INVESTIGATOR

Hôpital Foch

Jean-Marc Ayoubi

Role: STUDY_DIRECTOR

Hôpital Foch

Locations

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Hôpital Foch

Suresnes, , France

Site Status

Countries

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France

Other Identifiers

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2018_0072

Identifier Type: -

Identifier Source: org_study_id

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