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Evaluation of the effects of endometrial scratching on angiogenic and anti-angiogenic growth factors

Evaluation of the effects of endometrial scratching on angiogenic and anti-angiogenic growth factors expression in unexplained repeated implantation failure (uRIF) patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210316050723N1
Enrollment
20
Registered
2021-07-12
Start date
2021-06-20
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Unexplained repeated implantation failure (uRIF). Female infertility, unspecified

Interventions

Intervention 1: Intervention group: In the intervention group, endometrial sampling is obtained twice by Pipelle [one in the follicular phase (during 8-11 days and the last in the luteal phase (during

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Infertile women with unexplained repeated implantation failure (unknown definite causes of RIF) failed to conceive after three or more embryo transfer cycles using high-quality transferred embryos (at least one blastocyst ET cycle) Age of 20 to 40 years Body mass index (BMI) less than 25 kg/m2 Good response to stimulation of previous ovulation Having at least two embryos with good grade normal uterus results of hysterosalpingography (HSG) or hysteroscopy Participant consent was required to join in the study and to complete the consent form

Exclusion criteria

Exclusion criteria: The thickness of the endometrium on the day of Human chorionic gonadotropin hormone injection is less than 7 mm Women with congenital anomalies, intramural and subserosal myomas( larger than 5 cm) Submucosal myoma Women with endometrioma larger than or equal to 3 cm With adhesions With hydrosalpinx Have previous uterine or ovarian surgery Severe male factor infertility (sperm extraction from the testis, sperm freezing, sperm DNA fragmentation index equal to or above 16%) Patients with any specific medication If the number of available embryos is less than 2 in the current cycle Women with endometrial tuberculosis and those undergoing tuberculosis treatment Have a history of diabetes, thyroid disease, any endocrine, genetic, infection or autoimmune disorder Abnormal Pre-implantation Genetic Test (PGT) Results Any specific medication Failure to return the patient to prepare an endometrial sample Women with severe pain during obtaining of tissue samples or the possibility of infection

Design outcomes

Primary

MeasureTime frame
Evaluation of gene expression. Timepoint: In the endometrial sample obtained in the luteal phase during days 19-23. Method of measurement: Using PCR Array method and based on the copy number.

Secondary

MeasureTime frame
Clinical pregnancy. Timepoint: 5 weeks after embryo transfer. Method of measurement: Vaginal ultrasonography (observing the gestational sac and fetal heart rate).;Implantation. Timepoint: 5 weeks after embryo transfer. Method of measurement: The number of observed sacs divided by the number of transferred embryos.;Total dose of gonadotropin (IU). Timepoint: From ovarian stimulation to human chorionic gonadotropin (hCG) injection. Method of measurement: The number of international units (IU) received during the ovarian stimulation cycle.;Duration of ovarian stimulation (day). Timepoint: From the start of gonadotropin administration to human chorionic gonadotropin (hCG) injection. Method of measurement: According to the patient's monitoring ultrasound chart (number of days receiving the medicine).;Number of retrieved oocytes. Timepoint: On the day of oocyte pick-up. Method of measurement: The number of retrieved oocytes reported in the embryology chart.;Metaphase II oocytes. Timepoint: On the day of oocyte pick-up. Method of measurement: Based on the presence of the polar body reported by the embryologist.;Number of embryos. Timepoint: Three or five days after oocyte pick-up. Method of measurement: The number of cleavage embryos reported by the embryologist.;Embryo transfer cancelation. Timepoint: Three or five days after oocyte pick-up. Method of measurement: Participants with no embryo transfer.;Chemical pregnancy rate/Embryo transfer. Timepoint: 2 weeks after embryo transfer. Method of measurement: Beta human chorionic gonadotropin (beta hCG) titer in blood serum by ELISA method.;Blighted ovum/Embryo transfer. Timepoint: 5 weeks after embryo transfer. Method of measurement: Absence of fetus in gestational sac according to ultrasound report.;Ectopic pregnancy/Embryo transfer. Timepoint: 5 weeks after embryo transfer. Method of measurement: According to the ultrasound report, there is a gestational sac outside the uterus with a positive Beta hCG titer.;Miscarriage r

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrdad Bakhtiyari

Iran University of Medical Sciences

mehr_bakhtiyari@yahoo.com+98 21 8670 4567

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 12, 2026