Prospective Cohort Study of Robotic Assisted Laparoscopic Sacrocolpopexy Using MPATHY Restorelle Mesh

Urinary Incontinence Clinical Trial

— MPATHY  

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01320618
• Other study ID #: R09-06-003
• Status: Completed
• Phase: N/A
• First received: March 21, 2011
• Last updated: August 10, 2016
• Start date: May 2009
• Est. completion date: May 2011

Study information

• Verified date: August 2016
• Source: Atlantic Health System
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 120
• Est. completion date: May 2011
• Est. primary completion date: May 2011
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

• Any patient receiving Robotic assisted laparoscopic sacral colpopexy with polypropylene mesh

Exclusion Criteria:

• Other graft material than polypropylene mesh

• Enrollment in another study

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Enuresis
• Mesh Erosion
• Pelvic Organ Prolapse
• Prolapse
• Urinary Incontinence

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Atlantic Health System