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Home > Research > Clinical Trials > Endometrial Sampling (Pipelle)in IVF Patients. Clinical trial #NCT00411021
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Endometrial Sampling (Pipelle)in IVF Patients

Conditions Phase Intervention Type
  • Infertility
N/A
Procedure
Pipelle (Endometrial Sampling)

View trial NCT00411021 on www.clinicaltrials.gov

No PatientsLikeMe members are eligible for this trial.

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Contacts

Please use the information below to contact the trial coordinators.

    Micha Baum, MD
    baumdr@zahav.net.il
×

Eligibility

Ages Eligible for Study
20 years to 45 years
Genders Eligible for Study
F

Keywords

Sponsors

Other
Sheba Medical Center

Inclusion Criteria

- Women undergoing IVF treatment

- Repeated Implantation failure

Exclusion Criteria

- PID or suspected PID

- Undiagnosed Irregular Bleeding

Detailed Description

A prospective cross-over randomized study aimed to test the hypothesis that local injury of the endometrium increases the implantation rate in the successive cycle. Seventy IVF patients will be randomly selected to undergo either endometrial biopsies or minimal cervical scratch on days 8-10 and 21-23 of their cycle, preceding the IVF treatment. If not pregnant, the women will continue for another IVF cycle, preceded by endometrial or cervical scratch complimentary to their procedure in the first cycle. The main major outcomes will include pregnancy rate, implantation rate, endometrial thickness, abortion rate, live births and embryo quality.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00411021

Overall Contact Backup

Micha Baum, MD
baumdr@zahav.net.il

Locations

  • IVF Unit, Sheba Medical Center
    Ramat-Gan, Israel
    (Recruiting)

    Contact info

    Micha Baum, MD
    baumdr@zahav.net.il

Learn more at ClinicalTrials.gov

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