NCT02927548

Completed

Evaluation of the Efficacy and Safety of Advantage® Strips i...

Centre Hospitalier Universitaire de Nīmes Source

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Other study identifiers

Sponsor study identifier

IRB 15 01 06

Study Type

observational

Actual enrollment (reported)

500

Locations

1 country

Sites

1

Timeline

Study Start

January 2005

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

June 2012

Actual (reported)

Study Completion

March 2015

Actual (reported)

Brief Summary

This is a single-center retrospective study that evaluates the effectiveness and long-term safety of the TVT tape ( advantage Boston Scientific) in the treatment of stress urinary incontinence in women on a population of 500 patients with a mean follow-up of 6 years.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 500 participants
Study completion date: March 2015
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
January 2005
Date type not reported
This date has not been verified as actual or estimated.
Primary Completion
June 2012
Actual (reported)
Study Completion
March 2015
Actual (reported)
First Submitted
September 14, 2016
Actual (reported)
First Posted
October 7, 2016
Actual (reported)

Last Updated: June 18, 2026
Status Verified: September 2016
Last Update Submitted: June 17, 2026

Conditions

Urinary Incontinence

Outcome Measures

Primary Outcomes (3)

Patient global improvement scale
6 years
Complications
6 years
Urinary symptom questionnaire
6 years

Eligibility Criteria

Age29 Years - 89 Years

Sexfemale

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

patient of CHU Nîmes

You may qualify if:

patient who received the laying of a strip ADVANTAGE between 1/1/2015 and 1/6/2012

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Centre Hospitalier Universitaire de Nīmes
Otherlead

Study Sites (1)

CHU de Nîmes

Nîmes, Gard, 30029, France

MeSH Terms

Conditions

Urinary Incontinence

Condition Hierarchy (Ancestors)

Urination DisordersUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesLower Urinary Tract SymptomsUrological ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Enrollment

500 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: RETROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

September 14, 2016

First Posted

October 7, 2016

Study Start

January 2005

Date type not reported

This date has not been verified as actual or estimated.

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NCT00178191

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NCT00323245

Regaining Bladder Control in Postmenopausal Women With Osteoporosis

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NCT00333073

Effectiveness and Safety of Bulkamid® as Bulking Agent for the Treatment of Female Urinary Incontinence

Not ApplicableCompleted

Primary Completion

June 2012

Actual (reported)

Study Completion

March 2015

Actual (reported)

Last Updated

June 18, 2026

Record last verified: 2016-09

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT02927548
Data provider: ClinicalTrials.gov
Source updated: 2026-06-18
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:28:08 UTC

Locations

FR(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Outcome Measures

Primary Outcomes (3)

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Enrollment

Study Design

Study Record Dates

Source record

Locations