Endometrial Sampling (Pipelle)in IVF Patients

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00411021

Enrollment

Registered

2006-12-13

Start date

Unknown

Completion date

Unknown

Last updated

2006-12-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility

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.

Interventions

PROCEDUREPipelle (Endometrial Sampling)

Study design

Allocation

RANDOMIZED

Intervention model

CROSSOVER

Primary purpose

TREATMENT

Masking

SINGLE

Eligibility

Sex/Gender

FEMALE

Age

20 Years to 45 Years

Healthy volunteers

Yes

Inclusion criteria

* Women undergoing IVF treatment * Repeated Implantation failure

Exclusion criteria

* PID or suspected PID * Undiagnosed Irregular Bleeding

Countries

Israel

Contacts

Primary ContactMicha Baum, MD

baumdr@zahav.net.il

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026