Clinical Trials Directory

Trials / Completed

CompletedNCT06684951

Effects of Intrauterine Flushing With Human Chorionic Gonadotropin on ICSI Outcome

Study the Effects of Intrauterine Flushing With Low Dose Human Chorionic Gonadotropin on Ultrasound Parameter and Immunological Marker of Endometrial Receptivity of Infertile Female Undergoing ICSI Cycle

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Omayma Ismail Khalaf · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

a number of infertile women who were prepared for ICSI and immediately post ova pick up intrauterine flushing with human chorionic gonadotropin was done to study the effect of this drug on ICSI outcome and ultrasound parameter.

Detailed description

Ninety infertile women included. Written informed consent was obtained before being included in the study. Three groups of patients according to type of intervention. Assessment of plasma hormone level was done for all. The quantification of serum TNF and IL-10 levels was conducted through the application of the enzyme-linked immunosorbent assay (ELISA) methodology at a privately-owned laboratory.

Conditions

Interventions

TypeNameDescription
DRUGhCGobserve hCG effect on endometrial receptivity

Timeline

Start date
2022-10-23
Primary completion
2024-01-23
Completion
2024-04-30
First posted
2024-11-12
Last updated
2025-09-19
Results posted
2025-04-27

Locations

1 site across 1 country: Iraq

Regulatory

Source: ClinicalTrials.gov record NCT06684951. Inclusion in this directory is not an endorsement.