MedTrace Logo

Prospective Observational Prolapse Study

NCT04701047 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2025-01-15

No results posted yet for this study

Summary

The rationale of the study is to investigate the results of a prolapse treatment in adult women with a vaginal prolapse. The investigators will investigate this by taking questionnaires in women undergoing a surgical prolapse repair and in women that are being treated by a vaginal pessary. The objective is to compare the results of the different methods with each other and to observe the evolution of the symptoms in patients undergoing surgery or pessary use. The investigators would also like to discover existing problems in pessary use and adverse effects.

Conditions

  • Vaginal Prolapse

Interventions

DEVICE

vaginal pessary

insertion and follow up of a vaginal pessary

PROCEDURE

Vaginal prolapse surgery

surgery and follow up after vaginal prolapse surgery

Sponsors & Collaborators

  • University Hospital, Ghent

    lead OTHER

Principal Investigators

  • Tjalina Hamerlynck · UZ Gent

  • Steven Weyers · UZ Gent

  • Van Wessel Steffi · UZ Gent

  • Abosi Appeadu Kessewa · UZ Gent

  • Decalf Veerle · UZ Gent

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-03
Primary Completion
2028-01-31
Completion
2028-01-31

Countries

  • Belgium

Study Locations

More Related Trials

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 NCT04701047 on ClinicalTrials.gov