The Relevance Between the Level of Fetal Hemoglobin & Short-term

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05735717` - MT2021-08T Cell Receptor Alpha/Beta Depletion PBSC Transplantation for Heme Malignancies	Phase 2
Completed	`NCT01715480` - Effect of Broccoli Sprouts Homogenate on SS RBC	N/A
Recruiting	`NCT04802629` - Fetal Haemoglobin and Cerebral and Peripheral Oxygenation.
Completed	`NCT03764813` - Cord Blood Transfusion In Preterm Neonates (CB-TrIP)

See also

Status

Clinical Trial

Phase

Recruiting

NCT05735717 - MT2021-08T Cell Receptor Alpha/Beta Depletion PBSC Transplantation for Heme Malignancies

Phase 2

Completed

NCT01715480 - Effect of Broccoli Sprouts Homogenate on SS RBC

N/A

Recruiting

NCT04802629 - Fetal Haemoglobin and Cerebral and Peripheral Oxygenation.

Completed

NCT03764813 - Cord Blood Transfusion In Preterm Neonates (CB-TrIP)

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	NCT05788562
Study type	Observational
Source	The First Hospital of Jilin University
Contact	Qu Yangming
Phone	15844092520
Email	quym@jlu.edu.cn
Status	Not yet recruiting
Phase
Start date	April 1, 2023
Completion date	May 30, 2024

The Relevance Between the Level of Fetal Hemoglobin and Short-term Complications in Extremely Preterm Infants

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms