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ART Cycle Outcomes When Only 1 to 3 Oocytes Are Retrieved (POR)

I

Istituto Clinico Humanitas

Status

Completed

Conditions

Infertility Assisted Reproductive Technology
Oocyte Retrieval

Treatments

Procedure: Oocyte Retrieval

Study type

Observational

Funder types

Other

Identifiers

NCT06950476
POOR RESPONDERS

Details and patient eligibility

About

This is a monocentric retrospective observational study. The study focuses on the women who underwent Assisted Reproductive Technology (ART) cycles with poor ovarian response (POR), defined as <4 oocytes retrieved.

The objectives of the study are as follows:

  • Evaluate clinical pregnancy rate (CPR) and cumulative live birth rate (CLBR) in women with poor ovarian response.
  • Evaluate abortion rate in women with poor ovarian response.
  • Evaluate the influence of patient characteristics (age, Anti-Müllerian hormone [AMH] levels, Antral Follicle Count [AFC], Follicle Stimulating Hormone [FSH], Body Mass Index [BMI]) on women with poor ovarian response.

To address the study objectives, data will be collected using a specific internal web-based database. All oocyte retrieval procedures performed at the Humanitas Fertility Center from January 2010 to December 2023 will be included in the evaluation. Outcomes will be expressed in terms of CLBR, CPR and Abortion Rate.

Enrollment

3,761 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • The study database will include all women who underwent IVF treatment between 2010 and 2023 and were classified as poor ovarian responders, defined as those who retrieved fewer than 4 oocytes following controlled ovarian stimulation.

Exclusion criteria

  • The study database will exclude women who underwent IVF treatment and retrieved more than 3 oocytes following controlled ovarian stimulation.

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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