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Comparisons of Clinical Outcomes Between Novel Tailored Transvaginal Mesh Surgery and Vaginal Native Tissue Repair Surgery for Pelvic Organ Prolapse

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National Taiwan University

Status

Unknown

Conditions

Pelvic Organ Prolapse

Treatments

Procedure: Pelvic organ prolapse surgery without mesh
Procedure: Pelvic organ prolapse surgery with mesh

Study type

Observational

Funder types

Other

Identifiers

NCT02465710
201504023RINC

Details and patient eligibility

About

The issue of whether utilizing the mesh in the surgical treatment of pelvic organ prolapse remained undetermined.Thus, the aim of this study is to analyze clinical outcome of women who underwent pelvic organ prolapse surgeries with and without mesh implantation in the Department of Obstetrics & Gynecology of National Taiwan University Hospital.

Full description

Hypothesis / aims of study:

The use of mesh for women with pelvic organ prolapsed (POP) remains under debate, despite a recent randomized trial reported a favourable anatomic outcome of transvaginal mesh (TVM) surgery for cystocele, compared with anterior colporrhaphy. Besides, the issue of preserving uterus or not in women with POP during operation is still undetermined. Thus, the aim of this study is to compare clinical outcomes of the novel tailored TVM surgeries and conventional transvaginal native tissue repair (NTR) surgeries for POP.

Study design, materials and methods:

Between November 2011 and September 2014, the medical records of all consecutive women who underwent POP surgeries in a medical centre were reviewed. The choice of surgery method was according to the surgeons' preference. Clinical characteristics and intraoperative data and postoperative clinical outcomes were recorded. Wilcoxon rank-sum test was used to compare the data between two groups. Kaplan-Meier survival analysis was used to compare the recurrence rate between two groups.

Enrollment

350 estimated patients

Sex

Female

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All women who underwent surgical treatment of pelvic organ prolapse were enrolled in this study.
  • ≥ 20 years old female.

Exclusion criteria

  • Healthy women
  • Without underwent surgical treatment of pelvic organ prolapse

Trial design

350 participants in 1 patient group

pelvic organ prolapse
Description:
All women who underwent surgical treatment of pelvic organ prolapse in this study.
Treatment:
Procedure: Pelvic organ prolapse surgery with mesh
Procedure: Pelvic organ prolapse surgery without mesh

Trial contacts and locations

1

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Central trial contact

Ho-Hsiung Lin, MD,PhD; Sheng-Mou Hsiao

Data sourced from clinicaltrials.gov

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