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Endometrial Biopsy Protocol for In Vitro Fertilization (IVF)

K

Kaplan Medical Center

Status

Unknown

Conditions

Infertility
Recurrent Implantation Failure

Treatments

Procedure: endometrial biopsy/ies

Study type

Interventional

Funder types

Other

Identifiers

NCT01278706
kmc110154CTIL

Details and patient eligibility

About

Endometrial biopsy has been shown to improve IVF pregnancy and live birth rates. The optimal time of performing the biopsy is yet to be established.

In this study, the investigators will compare different temporal timing of the biopsies with regards to the menstrual cycle and their affect on the success rates of the treatment.

Enrollment

200 estimated patients

Sex

Female

Ages

18 to 38 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • normal menstrual cycle
  • between 1-6 previous failed IVF cycles
  • normal hormonal profile

Exclusion criteria

  • intrauterine procedure in last 3 months
  • hydrosalpinx
  • intrauterine lesion /malformation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 4 patient groups

no treatment
No Intervention group
one biopsy, proliferative phase
Experimental group
Treatment:
Procedure: endometrial biopsy/ies
one biopsy, secretory phase
Experimental group
Treatment:
Procedure: endometrial biopsy/ies
two biopsies
Experimental group
Treatment:
Procedure: endometrial biopsy/ies

Trial contacts and locations

2

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Central trial contact

Irit Granot, Ph.D.; Dan Levin, M.D.

Data sourced from clinicaltrials.gov

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