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Evaluation of intrauterine injection of recombinant human chorionic gonadotropin in improvement of pregnancy rates in in vitro fertilization/intracytoplasmic sperm injection

Evaluation of intrauterine injection of recombinant human chorionic gonadotropin before embryo transfer in improvement of implantation and pregnancy rates in in vitro fertilization/intracytoplasmic sperm injection: a prospective randomised controlled trial study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012121711790N1
Enrollment
182
Registered
2012-12-28
Start date
2011-11-22
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

Female Infertility. Female infertility

Interventions

Intervention 1: Intervention group: receiving 250 µg of rhCG as intrauterine injection 12 minutes before ET. Intervention 2: Control group: undergoing ET without a previous intrauterine injection of r
Treatment - Drugs
Intervention group: receiving 250 µg of rhCG as intrauterine injection 12 minutes before ET.

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 40 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria: female age under 40 years old with infertility. Exclusion criteria: previous IVF/ICSI trials, including a successful trial, endometriosis, azoospermia, uterine myoma or previous myomectomy, or the existence of hydrosalpinges.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Implantation rate. Timepoint: two weeks after embyo transfer. Method of measurement: conventional pregnancy test.;Clinical pregnancy rate. Timepoint: three weeks after a positive pregnancy test. Method of measurement: ultrasound.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoumeh Younesi

Shiraz University of Medical Sciences

younesim@sums.ac.ir ; younesi.dr@gmail.com+98 71 1646 2974

Outcome results

None listed

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