NCT02173444

Brief Summary

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

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
820

participants targeted

Target at P75+ for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2013

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2013

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

June 23, 2014

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 25, 2014

Completed
Last Updated

June 25, 2014

Status Verified

June 1, 2014

Enrollment Period

9 months

First QC Date

June 23, 2014

Last Update Submit

June 23, 2014

Conditions

Keywords

in-vitro fertilizationovarian stimulation

Outcome Measures

Primary Outcomes (2)

  • Number of oocytes

    At the time of oocyte retrieval

  • number of oocytes at time of oocyte retrieval

    up to 14 days

Interventions

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age ≤ 45 years at the time of FSH starting
  • BMI \< 25 kg/m2,
  • First IVF attempt
  • Receiving GnRH-antagonist protocol
  • Had oocyte retrieval

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

An Sinh Hospital

Ho Chi Minh City, Ho Chi Minh, Vietnam

Location

MeSH Terms

Conditions

Infertility

Interventions

Hematologic Tests

Condition Hierarchy (Ancestors)

Genital DiseasesUrogenital Diseases

Intervention Hierarchy (Ancestors)

Clinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisInvestigative Techniques

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctor

Study Record Dates

First Submitted

June 23, 2014

First Posted

June 25, 2014

Study Start

January 1, 2013

Primary Completion

October 1, 2013

Last Updated

June 25, 2014

Record last verified: 2014-06

Locations