Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
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.
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.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| unilateral suture sacro-hysteropexy | Active Comparator | patients in this group will undergo unilateral sacrouterine ligament plication with nonabsorbable suture and unilaterally suspended to the anterior longitudinal ligament. |
|
| bilateral suture sacro-hysteropexy | Active Comparator | patients in this group will undergo bilateral sacrouterine ligament plication with nonabsorbable sutures and bilaterally suspended to the anterior longitudinal ligament. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| unilateral suture sacro-hysteropexy | Procedure | patients in this group will undergo unilateral sacrouterine ligament plication with nonabsorbable suture and unilaterally suspended to the anterior longitudinal ligament. |
| Measure | Description | Time Frame |
|---|---|---|
| anatomical success of the operations | comparition of preoperative and postoperative pelvic organ prolapse quantification system (POP-Q) measurements of the patients | changes at 1 and 3 months after surgery |
| Measure | Description | Time Frame |
|---|---|---|
| evaluation of the sexual functions of the patients | comparition of preoperative and postoperative FSFI(female sexual function index) scores of the patients | changes at 1 and 3 months after surgery |
Not provided
Inclusion Criteria:
Exclusion Criteria:
female
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Gamze Nur Cimilli Senocak | Ataturk University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Atatürk University | Erzurum | Palandöken | Turkey (Türkiye) |
Not provided
Not provided
Not provided
Not provided
Not provided
| bilateral suture sacro-hysteropexy | Procedure | patients in this group will undergo bilateral sacrouterine ligament plication with nonabsorbable suture and bilaterally suspended to the anterior longitudinal ligament. |
|
| ID | Term |
|---|---|
| D056887 | Pelvic Organ Prolapse |
| ID | Term |
|---|---|
| D011391 | Prolapse |
| D020763 | Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
Not provided
Not provided