Evaluation of Anatomical Results and Sexual Functions After Unilateral and Bilateral Laparoscopic Suture Sacro-hysteropexy Operations

Evaluation of Anatomical Results and Sexual Functions After Unilateral and Bilateral Laparoscopic Suture Sacro-hysteropexy Operations, a Prospective Randomised Study

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06341088

Enrollment

Registered

2024-04-02

Start date

2024-04-05

Completion date

2025-02-05

Last updated

2025-07-17

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

Conditions

Pelvic Organ Prolapse

Keywords

suture sacro hysteropexy, Pelvic Organ Prolapse

Brief summary

The study was planned as prospective and randomized. For the study, patients will be randomized into two groups as unilateral and bilateral suture sacro-hysteropexy operations.

Detailed description

The study was planned as prospective and randomized. For the study, patients will be randomized into two groups as unilateral and bilateral suture sacro-hysteropexy operations.Computerized random number table will be used as randomization method. Patients who agree to participate in the study and fulfill the inclusion criteria will be evaluated on the effects of prolapse on quality of life and sexual function before and after the surgical procedures and their complaints and satisfaction will be questioned. Surgical success and complications will be evaluated. Changes in the level of prolapse will be evaluated.

Interventions

PROCEDUREunilateral suture sacro-hysteropexy

patients in this group will undergo unilateral sacrouterine ligament plication with nonabsorbable suture and unilaterally suspended to the anterior longitudinal ligament.

PROCEDUREbilateral suture sacro-hysteropexy

patients in this group will undergo bilateral sacrouterine ligament plication with nonabsorbable suture and bilaterally suspended to the anterior longitudinal ligament.

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 60 Years

Healthy volunteers

Yes

Inclusion criteria

1. Patients between the ages of 18-60 2. No previous prolapse surgery 3. Not having a chronic disease 4. Having stage 3-4 prolapse

Exclusion criteria

1. Outside the age range of 18-60 years 2. Previous prolapse surgery 3. Having early stage (1-2) prolapse 4. History of chronic disease

Design outcomes

Primary

Measure	Time frame	Description
anatomical success of the operations	changes at 1 and 3 months after surgery	comparition of preoperative and postoperative pelvic organ prolapse quantification system (POP-Q) measurements of the patients

Secondary

Measure	Time frame	Description
evaluation of the sexual functions of the patients	changes at 1 and 3 months after surgery	comparition of preoperative and postoperative FSFI(female sexual function index) scores of the patients

Countries

Turkey (Türkiye)

Outcome results

None listed

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