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RecruitingNCT06313411PRSUpdated Mar 15, 2024

How do I Perform a Laparoscopic Removal of a Pelvic Retroperitoneal Schwannoma

An observational study in Endometriosis Pelvic, sponsored by University Hospital, Strasbourg, France. Recruiting at 1 site in France. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-03-15.

Sponsored by University Hospital, Strasbourg, France · Observational

From the registry’s dates

  • Primary completion was expected by Apr 2024, 2 years 6 months ago, but the record still lists the study as recruiting.
  • Started Nov 2022; still recruiting 3 years 10 months later.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
1
Ages
18 Years and older
Sex
Female
01

Study summary

Schwannomas are mainly benign tumors, which develop mainly in the skull or in the cervical region. Retroperitoneal location is rare, since it represents between 0.5 and 5% of scwhanomas. The malignant retroperitoneal form is, however, more common than in other locations.

Retroperitoneal schwannoma is often discovered during the exploration of unexplained lumbo-pelvic pain, or in the face of compression of nearby organs. Abdominopelvic CT and magnetic resonance imaging are essential to characterize the mass and verify its extension. The precise diagnosis is based on the pathological examination of the part, and complete surgical excision is the standard treatment.

Acquiring the surgical techniques and skills necessary to carry out these types of procedures is essential to providing optimal patient care.

02

Conditions studied

  • Endometriosis Pelvic

Keywords

  • Endometriosis Pelvic
  • Schwannomas
03

In context

Neurilemmoma

82 studies on the registry are indexed under Neurilemmoma; 21 are open to participants now.

This study's planned enrollment of 1 is below the median of 63 across 30 observational studies indexed under Neurilemmoma.

Browse Neurilemmoma studies →

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 966 studies on the registry; 342 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Sampling method
Non-probability sample

Study population

  • Adult patient (≥18 years old) having received treatment at the Strasbourg University Hospital during 2021 for a retro-peritoneal pelvic carcinoma

Inclusion criteria

  • Adult patient (≥18 years old)
  • suffering from symptomatic deep pelvic endometriosis
  • having received treatment at the Strasbourg University Hospital during 2021 for a retro-peritoneal pelvic carcinoma
  • having not expressed, after information, the reuse of their data for the purposes of this research.

Exclusion criteria

Exclusion Criteria:

  • Patient who expressed her opposition to participating in the study
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
1 participant (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. laparoscopic removal of a retroperitoneal pelvic schwannoma

    The aim of this research is to train surgeons to perform laparoscopic removal of a retroperitoneal pelvic schwanoma

    Time frame: Through study completion, an average of 1 month

07

Study locations

1 of 1 sites recruiting
  • Service de Gynécologie Obstétrique - CHU de Strasbourg - France
    Strasbourg, 67091, France
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 15, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06313411
Lead sponsor
University Hospital, Strasbourg, France
Responsible party
Sponsor
First posted
Mar 15, 2024
Start date
Nov 23, 2022
Primary completion
Apr 2024 (estimated)
Completion
Apr 2024 (estimated)
Last update
Mar 15, 2024

Study contacts

Emilie FALLER, MD
Contact
emilie.faller@chru-strasbourg.fr
33 3 88 12 63 87

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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