How do I Perform a Laparoscopic Removal of a Pelvic Retroperitoneal Schwannoma
PRS
1 other identifier
observational
1
1 country
1
Brief 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.
Trial Health
Trial Health Score
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participants targeted
Target at below P25 for all trials
Started Nov 2022
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 23, 2022
CompletedFirst Submitted
Initial submission to the registry
December 14, 2023
CompletedFirst Posted
Study publicly available on registry
March 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2024
CompletedMarch 15, 2024
December 1, 2023
1.4 years
December 14, 2023
March 12, 2024
Conditions
Keywords
Outcome Measures
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
Through study completion, an average of 1 month
Eligibility Criteria
\- Adult patient (≥18 years old) having received treatment at the Strasbourg University Hospital during 2021 for a retro-peritoneal pelvic carcinoma
You may qualify if:
- 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.
You may not qualify if:
- Patient who expressed her opposition to participating in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Service de Gynécologie Obstétrique - CHU de Strasbourg - France
Strasbourg, 67091, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 14, 2023
First Posted
March 15, 2024
Study Start
November 23, 2022
Primary Completion
April 1, 2024
Study Completion
April 1, 2024
Last Updated
March 15, 2024
Record last verified: 2023-12