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Effect of human chorionic gonadotropin and embryo glue in infertility

Effect of intrauterine infusion of human chorionic gonadotropin and cultural environment of hyaluronan acid (embryo glue) on pregnancy outcomes in women with recurrent implantation failure

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221126056614N1
Enrollment
158
Registered
2023-02-22
Start date
2022-12-06
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Infertility. Complications associated with artificial fertilization

Interventions

Intervention 1: Intervention group: intrauterine infusion of human chorionic gonadotropin and embryo glue. In this group, 20 minutes before embryo transfer, 500 units of HCG (Pharmed Daru) and 15 micr

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Women who have a history of at least 3 failed transfer cycles or failed transfer of 4 good quality (grade A or B) embryos. Women who are in the frozen-thawed embryo transfer cycle and their preparation is done using estrogen and progesterone. Women who have at least one grade A or B embryo on the day of embryo transfer

Exclusion criteria

Exclusion criteria: Donated oocyte Donated embryo Surrogacy Presence of hydrosalpinx in hysterosalpingography or ultrasound History of uncontrolled endocrine diseases: diabetes, hypothyroidism and hyperthyroidism Male factor infertility (azoospermia) Difficult embryo transfer (needs manipulation of the cervix or under anesthesia) Uterine abnormalities Presence of severe endometriosis and endometrioma

Design outcomes

Primary

MeasureTime frame
Rate of Implantation. Timepoint: 5 weeks after intervention. Method of measurement: Ultrasound.;Rate of Abortion. Timepoint: 18 weeks after intervention. Method of measurement: Fetus excretion.;Rate of chemical pregnancy. Timepoint: 3-4 weeks after intervention. Method of measurement: Pregnancy test.;Rate of clinical pregnancy. Timepoint: 5 weeks after intervention. Method of measurement: Ultrasound.;Ongoing pregnancy. Timepoint: 38 weeks after intervention. Method of measurement: Delivery.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSepideh Peivandi

Mazandaran University of Medical Sciences

dr_peyvandi@yahoo.com+98 11 3336 1700

Outcome results

None listed

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