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A New Technique for Sacrospinous-Sacrotuberous Fixation for the Treatment of Uterovaginal and Vaginal Vault Prolapse

A New Technique for Sacrospinous-Sacrotuberous Fixation for the Treatment of Uterovaginal and Vaginal Vault Prolapse: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03487328
Enrollment
40
Registered
2018-04-04
Start date
2018-03-21
Completion date
2020-05-01
Last updated
2020-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Uterovaginal and Vaginal Vault Prolapse

Keywords

treatment

Brief summary

This prospective interventional randomized controlled trial is conducted to compare a new technique for Sacrospinous-Sacrotuberous fixation with the traditional sacrospinous ligament fixation technique for treatment of uterovaginal and vaginal vault prolapse.

Interventions

PROCEDURESacrospinous-Sacrotuberous fixation

Sacrospinous-Sacrotuberous fixation

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

1. Age from 40 to 60 years. 2. POP Q stage III & IV 3. Uterovaginal prolapse. 4. Vaginal vault prolapse. 5. BMI \>35.

Exclusion criteria

1. Age \> 40 years or \< 60 years. 2. POP Q stage I or II. 3. BMI \< 35. 4. Previous repair of uterovaginal or vaginal vault prolapse. 5. Comorbidity with Stress Urinary Incontinence. 6. Presence of persistent risk factor increasing intra-abdominal pressure e.g. chronic chest conditions. 7. Any significant comorbidity or psychiatric disorder that would compromise patient's consent.

Design outcomes

Primary

MeasureTime frame
Number of participants with recurrence of uterovaginal and vaginal vault prolapse1 year

Secondary

MeasureTime frameDescription
blood lossintraoperative
Injury to surrounding structuresintraoperativeNumber of participants that experience injury of important surrounding structure intraoperative
operative timeintraoperative

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026