A Study to Evaluate Experiences with Holmium Laser Ablation of Genitourinary Mesh Erosion following Transvaginal Mesh Surgery for Incontinence or Prolapse

Overview

  • Study type

    Observational
  • Study IDs

  • Describes the nature of a clinical study. Types include:

    • Observational study — observes people and measures outcomes without affecting results.
    • Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
    • Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
  • Site IRB
    • Rochester, Minnesota: 18-003215
    Sponsor Protocol Number: 18-003215

About this study

This study aims to evaluate our experience with holmium laser ablation of genitourinary mesh erosion following transvaginal mesh surgery for incontinence or prolapse.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. If you need assistance understanding the eligibility criteria, please contact the study team.

See eligibility criteria

Inclusion Criteria:

  • A bladder mesh erosion that was subsequently managed with laser excision of the genitourinary mesh

Exclusion Criteria: 

  • None

Participating Mayo Clinic locations

Study statuses change often. Please contact us for help.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Daniel Elliott, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

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CLS-20425495

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