Ignite Creation Date:
2024-05-06 @ 7:08 PM
Last Modification Date:
2024-10-26 @ 3:01 PM
Study NCT ID:
NCT05908656
Status:
RECRUITING
Last Update Posted:
2024-04-05
First Post:
2023-06-08
Brief Title:
Implementation and Evaluation of a Rare Disease Algorithm to Identify Persons at Risk of Gaucher Disease Using Data From Electronic Health Records EHRs in the United States Project Searchlight
Sponsor:
Sanofi
Organization:
Sanofi
Study Overview
Official Title:
Implementation and Evaluation of a Rare Disease Algorithm to Identify Persons at Risk of Gaucher Disease Using Data From Electronic Health Records EHRs in the United States
Status:
RECRUITING
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This is a three-phase study comprising both retrospective and prospective components as follows
Phase I Deployment of Rare Disease Algorithm
A diagnostic screening algorithm was developed using advanced analytical methods to identify patients who have an increased likelihood of having Gaucher disease This tool will be applied to a health systems electronic health records EHR
The top 50 active patients per healthcare system will be identified as highly ranked by the RDA and moved to Phase II As three to four healthcare systems are expected to participate in this study between 150 to 200 persons are expected to be identified and included in Phase II
Phase II Retrospective review of medical records of highly ranked persons The listing of persons highly-ranked by the RDA from phase I will be forwarded to the study team within each participating healthcare system After reviewing the RDA reports and medical records of each highly ranked person study site personnel will determine eligibility for Phase III based on the relevant selection criteria listed in the section below
Phase III Prospective diagnostic testing Eligible persons or their parentguardian from Phase II will be contacted and asked to provide consent for inclusion into the study After consent is received blood samples will be collected and sent for Gaucher diagnostic testing Because of overlap in clinical symptoms between Gaucher disease and acid sphingomyelinase deficiency ASMD patients will also receive diagnostic testing for ASMD Results will be shared with study site personnel who will subsequently inform the study subject andor their parentguardian where appropriate of results It is anticipated that participation of a typical subject will be less than 3 months
Phase I Deployment of Rare Disease Algorithm
A diagnostic screening algorithm was developed using advanced analytical methods to identify patients who have an increased likelihood of having Gaucher disease This tool will be applied to a health systems electronic health records EHR
The top 50 active patients per healthcare system will be identified as highly ranked by the RDA and moved to Phase II As three to four healthcare systems are expected to participate in this study between 150 to 200 persons are expected to be identified and included in Phase II
Phase II Retrospective review of medical records of highly ranked persons The listing of persons highly-ranked by the RDA from phase I will be forwarded to the study team within each participating healthcare system After reviewing the RDA reports and medical records of each highly ranked person study site personnel will determine eligibility for Phase III based on the relevant selection criteria listed in the section below
Phase III Prospective diagnostic testing Eligible persons or their parentguardian from Phase II will be contacted and asked to provide consent for inclusion into the study After consent is received blood samples will be collected and sent for Gaucher diagnostic testing Because of overlap in clinical symptoms between Gaucher disease and acid sphingomyelinase deficiency ASMD patients will also receive diagnostic testing for ASMD Results will be shared with study site personnel who will subsequently inform the study subject andor their parentguardian where appropriate of results It is anticipated that participation of a typical subject will be less than 3 months
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| U1111-1280-8450 | REGISTRY | ICTRP | None |