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Endometrial Hysteroscopy and Curettage Prior to Embryo Transfer


N/A
18 Years
35 Years
Open (Enrolling)
Female
Infertility

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Trial Information

Endometrial Hysteroscopy and Curettage Prior to Embryo Transfer


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.


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

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Implantation rate

Principal Investigator

Joel Geslevich, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

HaEmek Medical Center

Authority:

Israel: Ministry of Health

Study ID:

3280105

NCT ID:

NCT00367367

Start Date:

December 2005

Completion Date:

Related Keywords:

  • Infertility
  • embryo transfer
  • hysteroscopy
  • curettage
  • iv-vitro fertilization
  • molecular markers
  • endometrial receptivity
  • endometrial dating
  • Infertility
  • Adenoma

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