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OpenTrials
Completed

NCT Number: NCT02994550

Influence of FSH/LH Ratio in Controlled Ovarian Stimulation

The aim of this study is to compare different FSH/LH ratios in controlled ovarian stimulation

Completed

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Key information

Age range

35 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Early Phase 1

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients undergoing IVF cycles in Cruces University Hospital.
  • Signed IVF and cryopreservation informed consent.
  • Age >35 and <40 years.
  • FSH levels <10 mIU/ml.

Exclusion criteria

  • When inclusion criteria are not fulfilled

Treatment and study plan

FSH/LH

Drug

Primary outcomes

  1. Pregnancy achievement

    Time frame: 3 months after drug administration

    To report our results in terms of pregnancy per embryo transfer

Sponsors and collaborators

Lead sponsor

Hospital de Cruces

Other

Registry information

Official study title

Influence of FSH/LH Ratio in Controlled Ovarian Stimulation ( 2/1 Ratio vs 4/1 Ratio) in >35 Years Women Undergoing IVF

Important dates

Study start
2017
Primary completion
2017
Study completion
2018
First posted
Dec 16, 2016
Registry last updated
Aug 4, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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