Other Clinical Trial - Effect of Dexamethasone on Fetal Heart Rate

Clinical Trial Description

prospective cohort study on Effect of dexamethasone on fetal heart rate variability in case of preterm labour ;

Study Design

Related Conditions & MeSH terms

Fetal Heart Rate or Rhythm Abnormality Affecting Fetus
Obstetric Labor, Premature

See also
Status	Clinical Trial	Phase
Completed	`NCT06031142` - A Home Telemonitoring System for Wearable Fetal-ECG and EHG Acquisition During Pregnancy
Recruiting	`NCT03232918` - Oxytocin and Fetal Heart Rate Changes	Phase 4
Completed	`NCT05369247` - Interval Versus Continuous Exercise During Pregnancy	N/A
Recruiting	`NCT05958446` - Fetal-Hope Study: Home Monitoring of Fetal Heart Rate in SSA+ Pregnant Women

See also

Status

Clinical Trial

Phase

Completed

NCT06031142 - A Home Telemonitoring System for Wearable Fetal-ECG and EHG Acquisition During Pregnancy

Recruiting

NCT03232918 - Oxytocin and Fetal Heart Rate Changes

Phase 4

Completed

NCT05369247 - Interval Versus Continuous Exercise During Pregnancy

N/A

Recruiting

NCT05958446 - Fetal-Hope Study: Home Monitoring of Fetal Heart Rate in SSA+ Pregnant Women

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT05374135
Study type	Observational
Source	Assiut University
Contact	Ereny W Youssif, Master
Phone	01004252510
Email	Erenywagih@gmail.com
Status	Recruiting
Phase
Start date	May 1, 2021
Completion date	December 2022

Effect of Dexamethasone on Fetal Heart Rate Variables In Case Of Imminent Preterm Labor

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms