Prospective Cohort Study of Robotic Assisted Laparoscopic Sacrocolpopexy Using MPATHY Restorelle Mesh
This study has been completed.
Information provided by (Responsible Party):
Jodie Komar, Atlantic Health System
First received: March 21, 2011
Last updated: August 2, 2012
Last verified: March 2011
Robotic approach to sacral colpopexy is a relatively new procedure. The literature is scarce in regard to long term outcome. This advanced procedure is offered at Morristown Memorial. This protocol will review the one year outcome of patients who underwent this procedure using a polypropylene mesh. These outcomes will include anatomical and quality of life measures.
Pelvic Organ Prolapse
||Observational Model: Cohort
Time Perspective: Retrospective
| Study Start Date:
| Study Completion Date:
| Primary Completion Date:
||May 2011 (Final data collection date for primary outcome measure)
|Ages Eligible for Study:
||21 Years and older
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
Our study population will be woman who underwent Robotic assisted laparoscopic sacral colpopexy at the Morristown Memorial Hospital for correction of pelvic organ prolapseusing synthetic polypropelene mesh.
- Any patient receiving Robotic assisted laparoscopic sacral colpopexy with polypropylene mesh
- Other graft material than polypropylene mesh
- Enrollment in another study
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No publications provided
||Jodie Komar, PI, Atlantic Health System
History of Changes
|Other Study ID Numbers:
|Study First Received:
||March 21, 2011
||August 2, 2012
||United States: Institutional Review Board
Keywords provided by Atlantic Health System:
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on September 11, 2014
Pelvic Organ Prolapse
Pathological Conditions, Anatomical
Lower Urinary Tract Symptoms
Signs and Symptoms