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Effect of recombinant HCG administration in infertile women with IVF procedure

Effect of recombinant HCG administration in follicular phase on clinical pregnancy rate in frozen cycles of infertile women.(Tehran,Omid infertility center,2014-2015

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015012020736N1
Enrollment
250
Registered
2015-12-16
Start date
2013-12-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

infertility. Inability to achieve a pregnancy sterility

Interventions

Intervention 1: for trial group|: 125 units Recombinant HCG will be injected Subcutaneously from 8th day of their period for 7 days of mensuration period. Daily injection of 25 mg progesterone and da
Treatment - Drugs
for trial group|: 125 units Recombinant HCG will be injected Subcutaneously from 8th day of their period for 7 days of mensuration period. Daily injection of 25 mg progesterone and daily usage of 80
Control group: Daily injection of projestron 25 mg and 800 milligrams progesterone suppository

Sponsors

Vice chancellor for research, Tehran University of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Infertile women who were IVF candidate; infertile women who was recipient of Freezing embryo; Exclusion criteria: having uterus fibroma; having polyps bigger than 2 cm; Having Mullerian anomaly;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Chemical pregnancy. Timepoint: after four weekes. Method of measurement: B-HCG , miliunit.

Secondary

MeasureTime frame
Clinical pregnancy. Timepoint: two weeks after intervention. Method of measurement: transvaginal ultrasound and FHR.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mahshad Forati Kashani

Tehran University of Medical science

mahshad1008@yahoo.com+98 21 8885 2539

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026