← Eichor
Study identifier: NCT05836844 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Pragmatic Evaluation of Performance and Safety of the Anchorsure® Transvaginal Device for Surgical Treatment of Apical Prolapse in Women

Condition: Prolapse; Female · Prolapse Uterovaginal · Prolapse; Cervix  ·  Sponsor: Centre Hospitalier Universitaire de Nīmes

PhaseN/A
Planned participants120
Who can joinFemale, 50 Years to no upper limit
Healthy volunteersNo

About this study

Pelvic Organ Prolapse affects 50% of parous women, and apical prolapse is one of the most common types of prolapse. Treatment for apical prolapse ranges from observation, non-surgical treatment or surgical repair. An anchoring device can reduce dissection and operative time and is meant to provide strong fixation whilst minimizing potential postoperative pain by avoiding neurovascular injuries. These potential advantages must be evaluated in terms of performance and safety. This cohort study will be on patients undergoing sacrospinous fixation with the Anchorsure® system with a follow-up of 36 months.

This description comes directly from the study's public registry record.

Talk to the study team

Renaud de TAYRAC, Professor  ·  +334 66 68 32 16  ·  renaud.detayrac@chu-nimes.fr

Anissa MEGZARI  ·  +334 66 68 42 36  ·  drc@chu-nimes.fr

Always discuss trial participation with your own doctor first.

Locations (4)

La Rochelle General HospitalLa Rochelle, FranceRecruiting
Lille University HospitalLille, FranceRecruiting
Kremlin-Bicêtre HospitalParis, FranceRecruiting
Clinique Sainte-AnneStrasbourg, FranceRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05836844