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Calistar A vs. Calistar S - Comparative Cohort Retrospective Analysis of Single Incision POP Systems

NCT03715803 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 217

Last updated 2020-03-20

Study results available
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Summary

The main objective of this study is to compare the initial outcomes and complication of two meshes implanted through a single incision to treat anterior and apical prolapses, Calistar A and a second-generation low weight mesh called Calistar S (Soft).

Conditions

  • Pelvic Organ Prolapse

Interventions

DEVICE

Calistar A mesh to treat anterior and apical POP

Single incision surgery using Calistar A mesh to treat anterior and apical pelvic prolapses

DEVICE

Calistar S mesh to treat anterior and apical POP

Single incision surgery using Calistar S to treat anterior and apical pelvic prolapses

Sponsors & Collaborators

  • Agustin Sampietro

    lead OTHER

Principal Investigators

  • Agustín Sampietro, Dr · Faculty of Medicine, University of Buenos Aires

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-10-25
Primary Completion
2019-08-20
Completion
2019-12-30

Countries

  • Argentina

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03715803 on ClinicalTrials.gov