Clinical Trials Directory

Trials / Completed

CompletedNCT03476759

Laparoscopic Tubal Adhesiolysis Versus IVF-ICSI

Laparoscopic Tubal Adhesiolysis Versus IVF-ICSI in Cases of Post Caesarean Section Adhesions, Which is the Best?

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
300 (actual)
Sponsor
Tanta University · Academic / Other
Sex
Female
Age
20 Years – 35 Years
Healthy volunteers
Not accepted

Summary

2groups with peritoneal adhesions after cesarean delivery will be allocated to either laparoscopic tubal adhesiolysis or to IVF/ICSI

Detailed description

This randomized clinical trial will be conducted at Tanta university hospitals in fertility and MIS units. Two hundred and fifty 2ry infertility patients with confirmed post C.S adhesions will be included in the study and those patients will be divided randomly in two groups: Group A: 125 patients will be undergoing laparoscopic tubal adhesiolysis and\\or tuboplasty then a widow of 12 months post operatively is given for natural conception. Group B: 125 patients will undergo IVF-ICSI procedures. The primary outcome measure of the study will be the rate of clinical pregnancy. Inclusion criteria: * patient's age not exceeding 35 years old * confirmed post caesarean section tubal adhesions (by diagnostic laparoscopy report or video CDs) as a solitary cause of their 2ry infertility. Exclusion criteria: * patient's age \>35 years * other causes of infertility as male factor contribution, any ovulatory or endocrinological disorder, * diagnosed any degree of endometriosis * patients with history of recurrent pregnancy loss. * couples with prolonged sexual abstinence for any reason Detailed explanation of the aims, procedures, steps and nature of the study for the participants will be done and a written consent will be signed by each patient before inclusion. After allocation laparoscopic tubal adhesions will be dissected and normal anatomy and function will be restored. In the other group IVF/ICSI will be commenced The follow up with both groups will extend to 1year or till pregnancy is aggrieved The outcomes of the study were pregnancy rates and affordability

Conditions

Interventions

TypeNameDescription
PROCEDURETubal adhesiolysis125 patients will undergo tubal adhesiolysis or tuboplasty
DRUGIVF/ICSI125 patients will undergo IVF-ICSI procedures.

Timeline

Start date
2018-05-01
Primary completion
2021-10-31
Completion
2021-10-31
First posted
2018-03-26
Last updated
2021-11-29

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03476759. Inclusion in this directory is not an endorsement.