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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02173444
Other study ID # 1234-DHYD
Secondary ID
Status Completed
Phase N/A
First received June 23, 2014
Last updated June 23, 2014
Start date January 2013

Study information

Verified date June 2014
Source Vietnam National University
Contact n/a
Is FDA regulated No
Health authority Vietnam: Ministry of Health
Study type Interventional

Clinical Trial Summary

Serum bio-markers have different prediction values for ovarian response during ovarian stimulation in-vitro fertilization


Recruitment information / eligibility

Status Completed
Enrollment 820
Est. completion date
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Age = 45 years at the time of FSH starting

- BMI < 25 kg/m2,

- First IVF attempt

- Receiving GnRH-antagonist protocol

- Had oocyte retrieval

Exclusion Criteria:

- Had ovarian stimulation or ovulation induction within 2 months prior to the study

- PCOS

- Had ovarian tumor or endometrioma

- Hyperprolactinemia

- Thyroid hormone disorders

- Pituitary failure

- Had other medical situations such as liver failure, renal failure, heart disease, diabetes, depression

- Had IVM

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Other:
Blood test


Locations

Country Name City State
Vietnam An Sinh Hospital Ho Chi Minh City Ho Chi Minh

Sponsors (1)

Lead Sponsor Collaborator
Vietnam National University

Country where clinical trial is conducted

Vietnam, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of oocytes At the time of oocyte retrieval No
Primary number of oocytes at time of oocyte retrieval up to 14 days No
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