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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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03901586
Acronym
RICHTER
Enrollment
88
Registered
2019-04-03
Start date
2018-12-01
Completion date
2019-04-30
Last updated
2019-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Genital Prolapse

Brief summary

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

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.

Interventions

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

OTHERQuality of life

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

OTHERGynecological assessment

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

Sponsors

Hopital Foch
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Long-term satisfaction of the Richter procedure4 monthsIt will be ask to the patients to evaluate their satisfaction of the procedure, base on a 4-answer scale (Not at all satisfied, Not very satisfied, Moderately satisfied, Fully satisfied)

Secondary

MeasureTime frameDescription
Long term anatomic impact of the procedure7 monthsAn optional gynecological consult is proposed to the patients
Post-operative complications7 monthsPost-operative complications will be collected and compared to the anatomic impact of the procedure and the patient satisfaction

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026