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Is the IVF Outcome Dependent on the Time Interval Between hCG Administration and Oocyte Retrieval?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02044445
Enrollment
154
Registered
2014-01-24
Start date
2009-11-30
Completion date
Unknown
Last updated
2014-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Subfertility

Keywords

IVF, hCG, oocyte retrieval, time interval

Brief summary

During controlled ovarian hyperstimulation (COH), human chorionic gonadotrophin (hCG) is administered to trigger the final follicular maturation before oocyte retrieval, in an attempt to mimic the physiologic effects of LH. The hCG is administered when more than three follicles ≥17mm in mean diameter have developed. The time interval between hCG administration and oocyte retrieval is of critical importance since the time after luteinizing stimulus is a period of intense processes including the start of luteinization, expansion of cumulus cells and oocyte meiotic maturation. The commonly practiced hCG administration time of 33 to 36 h in most IVF cycles aims to avoiding spontaneous ovulation before oocyte retrieval. However, several studies have shown that significantly more high quality embryos have been obtained with a prolonged hCG-to-oocyte interval of 38 h. It has been hypothesized that longer interval would be beneficial in improving oocyte quality and achieving optimal maturation. Currently there are no data on the effect of the time interval between hCG administration and oocyte retrieval on IVF outcome in GnRH antagonist cycles. The aim of this study is to determine whether there is any difference in in vitro fertilization outcome when oocyte retrieval takes place at 36 h or 38 h following hCG administration

Interventions

PROCEDUREOocyte retrieval will be performed 36 h or 38 h after hCG administration

Oocyte retrieval will be performed 36 h or 38 h after hCG administration

Sponsors

Aristotle University Of Thessaloniki
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 43 Years
Healthy volunteers
No

Inclusion criteria

* women undergoing fresh IVF cycle with recombinant FSH and GnRH antagonists * regular spontaneous menstrual cycle (24-35 days) * age ≤ 43 years * FSH ≤ 20 IU/L

Exclusion criteria

* History of previous ovarian surgery * Women with Stage III-IV Endometriosis * Women undergoing natural cycle IVF

Design outcomes

Primary

MeasureTime frame
retrieval rate (cumulus-oocyte complexes/ follicles> 11 mm)up to 38 h after hCG administration

Secondary

MeasureTime frame
Clinical pregnancy rate (evidence of intrauterine sac with fetal heart activity at 6-8 weeks of gestation)At 6-8 weeks of gestation
Total number of oocytes retrievedup to 38 h after hCG administration

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026