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Endometrial Scratch Injury in Women With Unexplained Infertility Undergoing IUI

Endometrial Scratch Injury Induced Higher Pregnancy Rate for Women With Unexplained Infertility Undergoing IUI With Ovarian Stimulation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02349750
Enrollment
154
Registered
2015-01-29
Start date
2010-01-31
Completion date
2013-01-31
Last updated
2015-01-29

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

Conditions

Unexplained Infertility

Keywords

Endometrial Scratch Injury, Unexplained infertility, intrauterine insemenation, ovulation induction

Brief summary

The study included 154 infertile women Patients received 100 mg of oral clomiphene citrate for five days starting on day 3 of the menstrual cycle, followed by daily injection of 150 IU of hMG and when more than two dominant follicles reached a diameter of 17 mm 5,000 IU of hCG was injected intramuscularly. Patients were randomly allocated into two equal groups: Group C received IUI without ESI and Group S had ESI using No.8 neonatal feeding tube and after 24 to 36 hours, IUI was performed. Successful pregnancy was con-firmed by ultrasound and patients had failed trial underwent another trial of IUI for a maximum of three trials.

Detailed description

The study included 154 infertile women with mean duration of infertility of 3.9±0.4 years. Patients received 100 mg of oral clomiphene citrate for five days starting on day 3 of the menstrual cycle, followed by daily injection of 150 IU of hMG and when more than two dominant follicles reached a diameter of 17 mm 5,000 IU of hCG was injected intramuscularly. Patients were randomly allocated into two equal groups: Group C received IUI without ESI and Group S had ESI using No.8 neonatal feeding tube and after 24 to 36 hours, IUI was performed. Successful pregnancy was con-firmed by ultrasound and patients had failed trial underwent another trial of IUI for a maximum of three trials.

Interventions

ESI using No.8 neonatal feeding tube

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

1\. Couple with unexplained infertility and assigned for IUI

Exclusion criteria

1. Woman's age of more than 40 years 2. Ovarian cyst detected in the ultrasound examination 3. Uterine lesions such as submucosal leiomyoma 4. A previous diagnosis of moderate to severe pelvic endometriosis 5. Women with body mass index ≥35 kg/m2 o 6. Women with signs of hyperandrogenemia dy

Design outcomes

Primary

MeasureTime frame
clinical pregnancy14 days after IUI

Outcome results

None listed

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