- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05075174
Effect of Progesterone Levels on 15th Day After Embryo Transfer in Early Miscarriage < 7 WG or Evolving Pregancy Rates
September 29, 2021 updated by: University Hospital, Montpellier
Progesterone level has been studied at days before embryo transfert.
But, progesterone blood level has not been studied 15 days after embryo transfert.
The aim of this study is to study progesterone level impact at 15 days after embryo transfert on evolving pregnanies or early miscarriages.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Anticipated)
540
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Noémie RANISAVLJEVIC, M.D., Ph.D
- Phone Number: 33 06 37 10 89 38
- Email: n-ranisavljevic@chu-montpellier.fr
Study Contact Backup
- Name: MARIE DUPORT PERCIER, assistante
- Phone Number: 33 0467336427
- Email: m-duportpercier@chu-montpellier.fr
Study Locations
-
-
-
Montpellier, France, 34295
- Recruiting
- Uhmontpellier
-
Contact:
- Noémie RANISAVLJEVIC, M.D., Ph.D
- Phone Number: 33 06 37 10 89 38
- Email: n-ranisavljevic@chu-montpellier.fr
-
Contact:
- MARIE DUPORT PERCIER
- Email: m-duportpercier@chu-montpellier.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 43 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
ART program in Montpellier hospital >18 years old Blood progesterone level 15 days after embryo transfert Pregnancy development know
Description
Inclusion criteria:
- ART program in Montpellier hospital
- age >18 years old
- Blood progesterone level 15 days after embryo transfert
- Pregnancy development know
Exclusion criteria:
- non uterine pregnancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
number of blood progesterone
Time Frame: 1 day
|
blood progesterone at day 15 after embryo transfert
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Noémie Ranisavljevic, M.D., Ph.D, University Hospital, Montpellier
- Principal Investigator: MARIE DUPORT PERCIER, University Hospital, Montpellier
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2020
Primary Completion (Actual)
September 1, 2021
Study Completion (Anticipated)
June 1, 2022
Study Registration Dates
First Submitted
September 18, 2021
First Submitted That Met QC Criteria
September 29, 2021
First Posted (Actual)
October 12, 2021
Study Record Updates
Last Update Posted (Actual)
October 12, 2021
Last Update Submitted That Met QC Criteria
September 29, 2021
Last Verified
September 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RECHMPL21_0564
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
NC
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.