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Clinical Trials in China / NCT07344623
Recruiting Observational

Factors Associated With Clinical Pregnancy Outcomes in Intrauterine Insemination (IUI) Cycles

NCT07344623 · tracked via the Priya Life Science China tracker
Sponsor
Chinese University of Hong Kong
Phase
Observational
Started
2026-01-13
Last updated
2026-05-11

Condition(s) studied

Reproductive Issues

Study summary

Hypotheses:

We hypothesize that variations in hormonal profiles (LH, estradiol, progesterone) during ovarian stimulation, follicular response, endometrial characteristics, and sperm quality parameters are significantly associated with clinical pregnancy outcomes in intrauterine insemination (IUI) cycles.

Aims

* To investigate the association between hormonal profiles on the trigger day (LH, estradiol, progesterone), follicular response, endometrial thickness, and sperm parameters with clinical pregnancy outcomes in IUI cycles.
* To develop and validate a predictive model for clinical pregnancy incorporating key determinants such as female age, hormonal response, endometrial characteristics, and sperm quality.
* To compare natural and gonadotropin-stimulated IUI cycles in terms of hormonal profiles, pregnancy outcomes, and cost-effectiveness.

Primary Outcome Clinical pregnancy rate (CPR), defined as the presence of a gestational sac with a fetal heartbeat on ultrasound at approximately 6 weeks of gestation following intrauterine insemination.

Secondary Outcomes

* Biochemical pregnancy rate.
* Ongoing pregnancy rate
* Live birth rate

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
42 Years
Healthy volunteers
No
Inclusion Criteria: * Couples who underwent at least one IUI-intrauterine insemination cycle. Exclusion Criteria: * Couples who used donor sperm. * Cases with missing core outcome data

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The Chinese University of Hong Kong Hong Kong China Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07344623 on ClinicalTrials.gov ↗ ← All trials in China