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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01762111
Other study ID # OVO-12-22
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date December 2012
Est. completion date December 2013

Study information

Verified date January 2022
Source Clinique Ovo
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The woman fertility decrease with the age and there is a closely link with the ovarian reserve, the number of available eggs in the ovaries. Therefore, it is important to evaluate the ovarian reserve with specific marker to have a better prediction of the response of the in vitro fertilization treatment and to have a better rate of pregnancy. Until now, a lot of clinical criteria (age, duration of the infertility, number of antral follicles) and biological (FSH, Oestradiol, Inhibin B, EFFORT test, number of the eggs at the retrieval day) was suggested to help for the estimation of the ovarian reserve. Since couple of years, the anti-müllerian hormone (AMH) is recognize to be one of the best ovarian reserve marker, it corresponding the number of antral follicles, it is more sensitive and predictive. Moreover, during the In-Vitro Fertilization, the anti-müllerian hormone can provide the weak responds at the stimulation and the reverse, the risk of excessive responds (hyperstimulation). To choose the gonadotropin doses to administrate (stimulation ovarian hormone) during an In-Vitro Fertilization protocol, we need to know the anti-müllerian hormone dosage. However, if the anti-müllerian hormone is recognize to evaluate the quantity of available eggs in the ovaries, his role to determine the quality of these eggs still discussed. The goal of this study is to verify if the serum anti-müllerian hormone (blood) is a good indicator for the quality of the reserve ovarian evaluating the impact of anti-müllerian hormone rate on the pregnancy rate and implantation rate, during stimulate In-Vitro Fertilization protocol.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 43 Years
Eligibility Inclusion Criteria: - All infertile patients aged between 18 and 43 years - Patients with a prescription for a stimulated In-Vitro Fertilization cycle Exclusion Criteria: - Presence of endocrine disease: diabetes, hyperprolactinemia, abnormal thyroid-stimulating hormone (TSH) or Cushing syndrome - Renal or hepatic impairment known

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Canada Clinique Ovo Montreal Quebec

Sponsors (1)

Lead Sponsor Collaborator
Clinique Ovo

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pregnancy rates Clinical pregnancy rates per cycle and per transfer 7 weeks
Secondary Cumulative pregnancy rates Cumulative pregnancy rates including all frozen embryo transfer 5 years
Secondary Number of eggs Number of eggs retrieve at the end of the stimulated in-vitro fertilization cycle 4 weeks
Secondary Number of embryos Number of embryos obtain at the end of the stimulated in-vitro fertilization cycle 4 weeks
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