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Early Luteal Progesterone Profile in IVF Patients Triggered With hCG

NCT03174691 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 161

Last updated 2019-08-06

No results posted yet for this study

Summary

Until now very little information exists regarding the early luteal serum progesterone profile after Human chorionic gonadotropin (hCG) trigger. This pilot study will help characterize the serum progesterone, 17-hydroxyprogesterone profiles in IVF patients and correlate progesterone, 17-Hydroxyprogesterone levels to ovarian follicles obtained after stimulation with exogenous gonadotropins.

Conditions

Interventions

DIAGNOSTIC_TEST

Blood collection

A total of ten (10) blood samples (2ml/each) will be collected during the study. Blood samples will be collected on the following days for subsequent analysis of LH, Estradiol, hCG, progesterone and 17-Hydroxyprogesterone.

Sponsors & Collaborators

  • Mỹ Đức Hospital

    collaborator OTHER

  • Vietnam National University

    lead OTHER

Principal Investigators

  • Tuong M Ho, MD · Research Center for Genetics and Reproductive Health Ho Chi Minh, Ho Chi Minh Vietnam

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
42 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-06-07
Primary Completion
2017-08-08
Completion
2017-08-08

Countries

  • Vietnam

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03174691 on ClinicalTrials.gov