CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 120 enrolled
Drug / intervention
endometrial injurydevice
Likely dose
Not stated in record
Key inclusion· 8
  • Age 20–35 years
  • BMI 18–29 kg/m²
  • Primary infertility for >2 years with planning for IVF or ICSI
  • Normal ovulation confirmed by previous ultrasound
Key exclusion· 3
  • History of previous laparotomy
  • History suggesting endometriosis
  • Chronic medical conditions (cardiac disease, diabetes, renal disease, etc.)

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02863198
NCT02863198N/ACompleted

Endometrial Injury for Unexplained Infertility: Randomized Case-control Study

Benha University·interventional·Posted Aug 11, 2016·Updated Mar 14, 2017

In Brief

A clinical study evaluating endometrial injury for Infertility. Completed, enrolled 120 participants across 1 site.

Detailed Summary

One hundred and twenty women with unexplained infertility were included in the study. Divided randomly into two groups: Group I: (60 patients): (control group) Group II (60 patients): (study group) All the patients received (CC) and human menopausal gonadotropin. On day 5 of the cycle, Doppler examination was performed to all patients. Also on day 5, but only for group (II) patients, local endometrial injury was performed. Doppler studies was repeated, for all our patients, on the same day of prescribing human chorionic gonadotropin

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsInfertility
CountriesEgypt
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedAug 11, 2016
Enrollment StartOct 1, 2013
Primary CompletionFeb 1, 2016
Study CompletionJul 1, 2016
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 9.9 years ago

Interventions

endometrial injurydevice

Endometrial injury was done only for patient of the study group. It was done on day 5, under complete aseptic conditions, no anesthesia, was given in most of cases. Endometrial local injury was performed on the posterior wall, midline, and 10-15 mm from the fundus using pipelle endometrial sampling (Pipelle).