Comparision of three different methods for egg maturation, in the double stimulation protocol, in the low responder patients.

Phase 1

• Conditions: Patients with predictive indicators of low ovarian response (according to Poseidon criteria) and who undergo double ovarian stimulation (Dual Stim).; Therapeutic area: Diseases [C] - Female diseases of the urinary and reproductive systems and pregancy complications [C13]

• Registration Number: EUCTR2021-001225-43-ES
• Lead Sponsor: Instituto Bernabeu

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-09-02
• Last Update Posted: 13 September 2021

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: Female
• Target Recruitment: 165

Inclusion Criteria

1. Age: less than or equal to 43 years old
2. Body Mass Index (BMI): < 32
3. Presence of both ovaries
4. Indication for Dual Stim protocol
5. Compliance with the criteria to undergo IVF treatment.
6. Clinical history, history and physical examination without alterations.
7. AMH and RFA results according to group 3 or 4 of the Poseidon classification and not older than 6 months before the signature of the consent.
8. Ability to participate and comply with the study protocol.
9. To have given written consent
10. Normal karyotype and fragile X
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 165
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1. Non-compliance with instructions and/or non-formalization of consents or legal requirements for IVF.
2. Concurrent participation in another study

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified