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NOT YET RECRUITING
NCT07615634
NA

The Efficacy and Safety of Female PRP Co-incubation With Sperm During (IUI) Cycles

Sponsor: Chinese University of Hong Kong

View on ClinicalTrials.gov

Summary

The investigators hypothesize that infertility patients undergoing IUI who receive female autologous platelet-rich plasma (PRP) co-incubation with husband's sperm would have higher clinical pregnancy rate. Primary outcome: To compare the incidence of clinical pregnancy outcome in those infertility patients undergoing IUI with female PRP co-incubation with husband's sperm group and non-PRP group. Secondary outcomes: * To evaluate the post-culture sperm parameters between the intervention group and control group * To evaluate the IUI parameter between the intervention group and control group * To evaluate the safeness between the female PRP co-incubation with husband's sperm in the IUI group and non-PRP group, including potential infection rate or other pregnancy outcomes such as miscarriage, multiple pregnancy, ectopic pregnancy and molar pregnancy

Official title: The Efficacy and Safety of Female Autologous Platelet-Rich Plasma (PRP) Co-incubation With Sperm During the Intrauterine Insemination (IUI) Cycles: A Prospective, Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 42 Years

Study Type

INTERVENTIONAL

Enrollment

288

Start Date

2026-05-21

Completion Date

2028-05-20

Last Updated

2026-05-29

Healthy Volunteers

No

Interventions

OTHER

non-PRP group (control group)

non-PRP group (control group): non-PRP in the conventional IUI

OTHER

PRP group (intervention group)

PRP group (intervention group): female PRP co-incubation with husband's sperm in the IUI

Locations (1)

The Chinese University of Hong Kong

Hong Kong, China