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A Study of Robotic Assisted Laparoscopic Sacral Colpopexy Using Alyte Mesh

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01320644
Acronym
ALYTE
Enrollment
150
Registered
2011-03-22
Start date
2010-08-31
Completion date
2012-08-31
Last updated
2016-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mesh Erosion, Pelvic Organ Prolapse, Urinary Incontinence

Keywords

Uterine prolapse, vaginal prolapse, mesh erosion, urinary incontinence, bowel symptoms

Brief summary

Robotic approach to sacral colpopexy is a relatively new procedure. The literature is scarce in regard to long term outcomes. This advanced procedure is offered at Morristown Memorial. THis protocol will review the one year outcome of patients who underwent this pocedure using a polypropylene mesh. These outcomes will incude anatomical and quality of life measures.

Interventions

None listed

Sponsors

Atlantic Health System
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Any patient receiving Robotic assisted laparoscopic sacral copopexy with polypropylene mesh * \>21 y.o

Exclusion criteria

* Graft material other than polypropylene mesh * Enrollment in another study

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026