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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02994550
Other study ID # CEIC E14/30
Secondary ID
Status Completed
Phase Early Phase 1
First received
Last updated
Start date January 2017
Est. completion date January 2018

Study information

Verified date August 2022
Source Hospital de Cruces
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 447
Est. completion date January 2018
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender Female
Age group 35 Years to 40 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
FSH/LH


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Hospital de Cruces

Outcome

Type Measure Description Time frame Safety issue
Primary Pregnancy achievement To report our results in terms of pregnancy per embryo transfer 3 months after drug administration
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