Effect of Dexamethasone on Fetal Heart Rate Variables In Case Of Imminent Preterm Labor
NCT ID: NCT05374135
Last Updated: 2022-05-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
97 participants
OBSERVATIONAL
2021-05-01
2022-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Dexamethasone on Fetal and Uteroplacental Doppler
NCT02662790
Effect of Pre-delivery Dexamethasone in Comparison With Betamethasone on Fetal Heart Trace
NCT07078786
A Clinical Pharmacological Study of Dose Halving of Dexamethasone in Pregnant Women With Preterm Labour With Preterm Birth at Greater Than or Equal to 34 Gestational Weeks (34GW+)
NCT06350565
Clinical Pharmacology of Dexamethasone in Pregnant Women With Preterm Labor
NCT05207852
Effect of Antenatal Corticosteroids on Neonatal Morbidity.
NCT03446937
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
15 Years
50 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Assiut University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ereny Wagih Youssif
Ereny wagih youssif
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Tarek Kh Al-Hussini
Role: PRINCIPAL_INVESTIGATOR
Assiut University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Assiut university
Asyut, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Tarek A Abdelradi, Professor
Role: CONTACT
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Assiut university
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Dexamethasone effect on FHR
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.