Endometrial Curettage Before Embryo Transfer

Not Applicable

• Conditions: Infertility

• Registration Number: NCT00367367
• Lead Sponsor: HaEmek Medical Center, Israel

Brief Summary

Studies have shown that endometrial sampling in the month prior to embryo transfer may increase pregnancy rates. We wish to test this hypothesis by performing a hysteroscopy and curettage in the month proceeding embryo transfer during IVF, IVF/ICSI or Frozen/Thawed cycles.

Detailed Description

It has been suggested that local injury to the endometrium doubles the rate of implantation and successful pregnancies in IVF patients.

Purpose

1. To determine whether performing curettage the month prior to embryo transfer (ET) increases the chance of embryo implantation.

2. To study molecular attributes of the endometrium taken at curettage and to compare them to those cycles resulting in pregnancy and those which do not result in pregnancy.

Samples will be grown as primary culture in the research laboratory and possible molecular markers and attachment assays for endometrial receptivity will be studied.

Patient selection: Patients undergoing IVF or IVF-ICSI at Ha'Emek medical center/ IVF unit. Woman over 35 years of age will be excluded since implantation failure is more likely to be due to genetic, chromosomal or cytoplasmic aberrations in their oocytes.

Proposed protocol:

1. Informed consent obtained from prospective candidates.

2. Participants randomly divided to three groups

1. Control group

2. Hysteroscopy and curettage performed on days 15-17 of menstrual cycle

3. Hysteroscopy and curettage performed on days 19-22 of menstrual cycle

3. After the following menses an IVF, IVF-ICSI, or frozen embryo cycle is performed according to the unit's standard protocols.

4. The primary end point of the study will be the implantation rate after ET and the expression of possible molecular markers for endometrial receptivity in the pregnant patients.

Study Timeline

• Study Start: 2005-12
• Status Verified: 2006-08
• Study First Submitted: 2006-08-20
• Study First Submitted QC: 2006-08-20
• Last Update Submitted: 2006-08-20
• Study First Posted: 2006-08-22
• Last Update Posted: 2006-08-22

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 90

Inclusion Criteria

• Informed consent
• In-vitro fertilization candidate
• Normal blood coagulation

Exclusion Criteria

• Anemia (hemoglobin under 10 mg/dl)
• Abnormal maternal karyotype
• Thrombocytopenia under 140,000
• Any contraindication to hysteroscopy or in-vitro fertilization

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Implantation rate
Pregnancy rate
Endometrial receptivity

Trial Locations

Locations (1)

Department of Obstetrics and gynecology, HaEmek Medical Center; 🇮🇱 Afula, Israel