Anterior Vaginal Wall Reconstruction

Sponsor
Hippocration General Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT00571350
Collaborator
(none)
50
1
1
35
1.4

Study Details

Study Description

Brief Summary

The purpose of this study is to assess the effectiveness of the polypropylene tape in preventing cystocele recurrence when placed underneath the bladder base as a concomitant measure to the anterior colporrhaphy procedure.

Condition or Disease Intervention/Treatment Phase
  • Procedure: tvt-o operation
  • Procedure: tvt o operation
Phase 1/Phase 2

Detailed Description

Objective: The purpose of this study is to assess the effectiveness of the polypropylene tape in preventing cystocele recurrence when placed underneath the bladder base as a concomitant measure to the anterior colporrhaphy procedure.

Methods: Fifty Caucasian women 50 to 77 years old (mean age 66.6 years), 2 pre and 48 post menopausal with stage II-IV pelvic organ prolapse, enrolled into the study. Vaginal reconstructive surgery included an anterior colporrhaphy in all patients, posterior colpoperineorrhaphy in 28 patients and hysterectomy in 36 patients. They were randomly divided in a control group of 22 women and a study group of 28 women. As reinforcement to the anterior colporrhaphy procedure a polypropylene tape (TVT-O) was placed not under the midurethra, as originally described in case of stress incontinence, but underneath the bladder base and was fixed there with polyglactin sutures, in the study group. The postoperative follow up was carried out in frequent intervals of 4 months (total 48 months). The assessment of the anatomic result included evaluation of the operated sites and of the position of the tapes inserted on clinical grounds and after perineal sonography, which measured the distance of the bladder base to the inferior edge of the symphysis pubis.

Results: In all patients the postoperative correction of the anterior vaginal wall was sufficient; the mean distance of the bladder base to the inferior edge of the symphysis pubis was 1.5 cm (range 1.0-2.2 cm). Mean residual urine volume was 30 ml. There were postoperatively 2 cases of stress incontinence and two cases of urge incontinence one in each group. There was no case of tape erosion noted, no dyspareunia and no recurrent cystocele in the study group. Four cases of recurrent cystocele (20%) were reported in our control group.

Conclusion: The tension free vaginal tape, particularly TVT-O, placed underneath the bladder base, when performed concomitantly to the anterior colporrhaphy appears to be safe and effective. While the preliminary results of our study are encouraging, larger series of patients and longer follow up are required to verify the effectiveness of the aforementioned modification.

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Anterior Vaginal Wall Reconstruction: Anterior Colporrhaphy Reinforced With Tension Free Vaginal Tape Underneath Bladder Base
Study Start Date :
Jan 1, 2005
Anticipated Study Completion Date :
Dec 1, 2007

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: A

women with vaginal prolapse who underwent TVT O

Procedure: tvt-o operation
transvaginal tention free obturator tape
Other Names:
  • Johnson & Johnson Ethicon Gyneacare, Somerville, NJ, USA
  • Procedure: tvt o operation
    transobturator vaginal tape insertion
    Other Names:
  • tention free vaginal tape
  • Outcome Measures

    Primary Outcome Measures

    1. The purpose of this study is to assess the effectiveness of the polypropylene tape in preventing cystocele recurrence when placed underneath the bladder base as a concomitant measure to the anterior colporrhaphy procedure. [2008]

    Secondary Outcome Measures

    1. GOOD QUALITY OF LIFE FOR PATIENTS [2008]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    50 Years to 77 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Women 50-77 years old with stage II-IV organ prolapse

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Medical School Aristotle University Thessaloniki Greece

    Sponsors and Collaborators

    • Hippocration General Hospital

    Investigators

    • Principal Investigator: ANGELOS DANIILIDIS, MD, HIPPOKRATIO UNIVERSITY HOSPITAL
    • Study Director: JOHN TZAFETTAS, PROFESSOR, HIPPOKRATIO UNIVERSITY HOSPITAL
    • Principal Investigator: THEOHARIS TANTANASIS, ASS PROF, HIPPOKRATIO UNIVERSITY HOSPITAL

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00571350
    Other Study ID Numbers:
    • ARISFC
    • HIPPOKRATIO HOSPITAL
    First Posted:
    Dec 12, 2007
    Last Update Posted:
    Dec 12, 2007
    Last Verified:
    Dec 1, 2007
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 12, 2007