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Pregnancy Rate in Women With Normal Uterine Cavity and Those With Corrected Uterine Lesions in ICSI Cycles

A

Assiut University

Status

Unknown

Conditions

Intracytoplasmic Sperm Injection

Treatments

Procedure: hysteroscopy

Study type

Observational

Funder types

Other

Identifiers

NCT03680690
pregnancy rate in ICSI cycles

Details and patient eligibility

About

The aim of the current study is to investigate the pregnancy rate in women with normal uterine cavity and those detected or corrected uterine cavitary lesions, assessed by hysteroscopy in ICSI cycles.

Full description

Intrauterine pathology has been reported in up to 25% of infertile women having IVF treatment and in as many as 50% of women with recurrent implantation failure, leading to suggestions that correction of such pathology could improve treatment outcome. Hysteroscopy allows visual assessment of the cervical canal and uterine cavity and provides the opportunity to operate in the same setting. Routine outpatient hysteroscopy before starting IVF has been postulated to diagnose and treat abnormalities of the cervix and uterine cavity and hence improve IVF outcome.

A systematic review of published studies suggested that outpatient hysteroscopy in the menstrual cycle preceding an IVF treatment cycle could significantly increase the clinical pregnancy rate in women who had previously had recurrent implantation failure, even when no hysteroscopic abnormality was detected.

However, the result of the TROPHY study - published in the Lancet in 2016 concluded that Outpatient hysteroscopy before IVF in women with a normal ultrasound of the uterine cavity and a history of unsuccessful IVF treatment cycles does not improve the livebirth rate and they recommended that further research into the effectiveness of surgical correction of specific uterine cavity abnormalities before IVF is warranted.

An MD thesis done in our department on the evaluation of the endometrial cavity in infertile patients and prior to IVF recommended that there is an urgent need to RCT to emphasize the benefit of removal of the detected intrauterine lesions before proceeding to IVF.

Enrollment

244 estimated patients

Sex

Female

Ages

18 to 38 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women between 18 and 38 years old.
  • An indication for IVF/ICSI.
  • Normal 2D transvaginal U/S assessment of the uterine cavity, or abnormal cavity detected by 2D ,3D and HSG.
  • Women with primary or secondary infertility.
  • Women with BMI between 20 & 35.

Exclusion criteria

  • Refusal to join the study.
  • Untreated tubal hydrosalpinges.
  • Poor responders as assessed by AFC 4 or less ,AMH O.8 ng/dl (nice 2013).

Trial design

244 participants in 2 patient groups

Group A
Description:
women with normal uterus,detected by hysteroscopy.
Treatment:
Procedure: hysteroscopy
Group B
Description:
Women with detected or corrected uterine cavitary lesions by hysteroscopy.
Treatment:
Procedure: hysteroscopy

Trial contacts and locations

0

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Central trial contact

Ahmed Kamel, MSc/Mbbh; Ahmed Youssef, MD/Mssc/Mbbh

Data sourced from clinicaltrials.gov

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