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Progesterone Supplementation on Women Having Low Progesterone Levels on Transfer Day

NCT04897269 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 824

Last updated 2023-12-11

No results posted yet for this study

Summary

The main objective of this study is to compare clinical pregnancy rates between two groups of women who have progesterone levels below 10 ng/mL on the day of frozen embryo transfer: group 1 (vaginal micronized progesterone supplemented with progesterone intramuscular 50 mg per day) and group 2 (vaginal micronized progesterone with no supplementation)

Conditions

  • Assisted Reproductive Technology

Interventions

PROCEDURE

Progesterone supplementation

This procedure is to add more progesterone on those who have low progesterone levels on the day of embryo transfer

Sponsors & Collaborators

  • Tu Du Hospital

    lead OTHER_GOV

Principal Investigators

  • Chau TM Le · Department of Infertility, Tu Du Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-05-20
Primary Completion
2024-05-20
Completion
2024-06-20

Countries

  • Vietnam

Study Locations

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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 NCT04897269 on ClinicalTrials.gov