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Double Trigger in Patients With Low Proportion of Mature Oocytes

Double Trigger in Patients With Low Proportion of Mature Oocytes. A Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04407052
Enrollment
66
Registered
2020-05-29
Start date
2020-05-30
Completion date
2021-02-02
Last updated
2020-05-29

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

Conditions

Infertility, Female

Keywords

IVF, HCG, GnRH agonist trigger

Brief summary

The aim of this randomized controlled trial is to determine whether co-administration of GnRH agonist and hCG for final oocyte maturation ( 40 and 34 h prior to oocyte retrieval , respectively) can increase the number of mature oocytes in patients with history of low proportion of mature oocytes in previous IVF cycle triggered by HCG.

Interventions

Final follicular maturation is triggered by the coadministration of GnRH-agonist (Triptorelin acetate, decapeptyl 0.2 mg, Slough, United Kingdom) and 10000 IU of HCG, 40 and 34 h prior to oocyte retrieval, respectively

Final follicular maturation is triggered by a dose of 10000 IU of HCG 36 h prior to oocyte retrieval

Sponsors

Riyadh Fertility and Reproductive Health center
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Patients with history of low proportion of mature oocytes in previous IVF attempt (triggered by HCG). * Patients with 6 to 15 mature follicles on the day oocyte trigger in the current IVF-ET attempt

Exclusion criteria

* Endometriosis * PCOS

Design outcomes

Primary

MeasureTime frame
Number of oocytes retrievedFirst day after oocyte retrieval

Secondary

MeasureTime frameDescription
Clinical pregnancy rateFirst 5 weeks after oocyte retrievalThe presence of gestational sac detected by ultrasound examination

Countries

Egypt

Contacts

Primary ContactUsama M Fouda, Prof.
umfrfouda@yahoo.com+201095401375

Outcome results

None listed

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