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Endometrial Sampling (Pipelle)in IVF Patients

Sponsor
Sheba Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT00411021
Collaborator
(none)
70
Enrollment
1
Location

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Pipelle (Endometrial Sampling)
 N/A

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single
Primary Purpose:
Treatment
Official Title:
Endometrial Sampling (Pipelle)in IVF Patients

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    • Women undergoing IVF treatment

    • Repeated Implantation failure

    Exclusion Criteria:

    • PID or suspected PID

    • Undiagnosed Irregular Bleeding

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 IVF Unit, Sheba Medical Center Ramat-Gan Israel 52621

    Sponsors and Collaborators

    • Sheba Medical Center

    Investigators

    • Principal Investigator: Micha Baum, MD, Sheba Medical Center, Israel

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00411021
    Other Study ID Numbers:
    • SHEBA-05-3674-MB-CTIL
    First Posted:
    Dec 13, 2006
    Last Update Posted:
    Dec 13, 2006
    Last Verified:
    Dec 1, 2006
    Additional relevant MeSH terms:
    Infertility

    Study Results

    No Results Posted as of Dec 13, 2006