Clinical Trials Directory

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UnknownNCT02430740

Tailored Ovarian Stimulation Based on BMI, AMH, AFC

Multicentric Randomized Controlled Study to Determine a Tailored Strategy for Controlled Ovarian Stimulation in IVF Based on AMH, BMI and AFC

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain · Academic / Other
Sex
Female
Age
18 Years – 43 Years
Healthy volunteers
Not accepted

Summary

The study objective is to develop a tailored based strategy for ovarian stimulation in IVF patients using AMH, BMI, antral follicle count (AFC). 300 patients will be randomized in 2 arms: 1. control group: standard care rec FSH. 2. study group: modified dose of Rec FSH based on AFC with a correction factor based on BMI and basal AMH level. Primary endpoints: number of mature follicles and eggs collected at egg retrieval; amount of rec FSH used. Secondary endpoints: fertilization rate; cleavage rate; clinical pregnancy rate; inhibin B and AMH levels during ovarian stimulation.

Detailed description

The study objective is to develop a tailored based strategy for ovarian stimulation in IVF patients using AMH, BMI, AFC and inhibin B. 300 patients will be stimulated with rec FSH and an antagonist pituitary inhibition protocol, and randomized (at random computer generated numbers) in 2 arms: 1. control group: standard care recFSH based on age, basal FSH and AFC. 2. study group: modified dose of Rec FSH based on AFC with a correction factor based on BMI and basal AMH level. FSH administration: 20IU per antral follicle (from 2-5mm) corrected as follows: Correction factor for AMH: \<1 pMol/L X4 1-6 pMol/L X2 7-18 pMol/L X1 \>18 pMol/L X0.5 BMI 16.5-18.5 X0.75 18.5-25 X1 25-30 X1.25 30-35 X1.5 35-40 X2 Primary endpoints: number of mature follicles and eggs collected at egg retrieval; amount of rec FSH used. Secondary endpoints: fertilization rate; cleavage rate; clinical pregnancy rate; inhibin B and AMH levels during ovarian stimulation.

Conditions

Interventions

TypeNameDescription
DRUGrecFSH

Timeline

Start date
2016-01-01
Primary completion
2023-12-01
Completion
2023-12-01
First posted
2015-04-30
Last updated
2023-04-12

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT02430740. Inclusion in this directory is not an endorsement.