Clin2
NCT07009821Worth exploringNot yet recruiting

Newborn screening for hemoglobin blood disorders

SCD

Part of Blood & lymphatic clinical trials.

This study will test newborns who may be at higher risk for inherited blood disorders (hemoglobinopathies) using a special screening program called EmoCamp. The goal is to catch these conditions early so babies can get the care they need.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
1,000 people
Ages
Any age
Study type
Observational

Who can take part

  • Your baby must be a newborn (just born).
  • Your baby must be thought to have a higher chance of having a hemoglobin disorder (like sickle cell disease or thalassemia).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT06615024Not yet recruiting
Screening healthy newborns for sickle cell and G6PD

This study screens healthy newborns for two inherited blood conditions: sickle cell disease and G6PD deficiency. It is meant to check if these conditions can occur together, which may help doctors provide better care.

NCT07206095Recruiting
Better diagnosis for inherited red blood cell diseases

This trial aims to improve how doctors diagnose rare inherited anemias, including sickle cell disease and other conditions that destroy red blood cells. It may help if you have a confirmed or suspected diagnosis but need more clarity through advanced testing.

Barcelona, Barcelona
NCT05990179Recruiting
Screening newborns for rare diseases using genetics

This trial offers free genetic screening for rare diseases in newborns. It aims to find health conditions early so babies can get the right care sooner.

New York, New York
NCT04393701Recruiting
Testing newborn blood spots to check for rare storage diseases

This pilot study tries a systematic way to look for several rare “lysosomal storage” diseases in newborns using a specialized lab test on routine blood samples. It may help detect these conditions earlier so treatment can start sooner if needed.

Caen
NCT05368038Enrolling by invitation
Newborn screening program for babies up to 4 weeks old

This trial tests a flexible newborn screening process that looks for certain conditions early in life. It may help by catching problems sooner, when treatment can be started earlier.

Brooklyn, New York
NCT06549218Recruiting
Genetic newborn screening for rare diseases

This study tests a new way to screen newborns for rare genetic diseases using a blood sample. It aims to find treatable conditions early so that babies can get care sooner.

Dijon

Hear when a new SCD trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.