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NCT05651113

The Experience of Screening for SCID

Recruiting now Last updated 14 December 2022
What this trial tests

trial testing SCID Screening in Severe Combined Immunodeficiency in 90 participants. Currently enrolling.

Timeline
9 November 2022
Primary endpoint
31 March 2029
31 March 2029

Quick facts

Lead sponsorKing's College London
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment90
Start date9 November 2022
Primary completion31 March 2029
Estimated completion31 March 2029
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

King's College London

Who can join

18 and older, any sex, with Severe Combined Immunodeficiency. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This project will evaluate the impact of including Severe Combined Immunodeficiency into the newborn bloodspot screening panel. It will recruit parents and health professionals primarily from the sites where this new form of screening is being trialled well as additional sites where clinicians will be involved in the care of these babies and comparator groups are needed. The proposed work will consist of two work packages. The first, a mixed-methods study conducted with families from the point of screening information being returned through to the child's fifth birthday. The second, a qualitative interview study conducted with health professionals during the clinical evaluation phase of the national pilot programme.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Severe Combined Immunodeficiency

Currently open trials in the same condition.

Other King's College London trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05651113.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing