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Influence of FSH/LH Ratio in Controlled Ovarian Stimulation

C

Cruces University Hospital

Status and phase

Completed
Early Phase 1

Conditions

Sub-Fertility

Treatments

Drug: FSH/LH

Study type

Interventional

Funder types

Other

Identifiers

NCT02994550
CEIC E14/30

Details and patient eligibility

About

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

Enrollment

447 patients

Sex

Female

Ages

35 to 40 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

447 participants in 2 patient groups

FSH/LH 2/1
Experimental group
Description:
dose: 300IU FSHrec and 150IU LHrec
Treatment:
Drug: FSH/LH
FSH/LH 4/1
Experimental group
Description:
dose: 300IU FSHrec and 75IU LHrec
Treatment:
Drug: FSH/LH

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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