Skip to main content
MedPathMedPath Home
Clinical Trials/NCT06490510
NCT06490510
Completed
Not Applicable

Prognostic Significance of Mutation Type and Chromosome Fragility in Fanconi Anemia

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau1 site in 1 country227 target enrollmentMay 16, 2024
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsFanconi Anemia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fanconi Anemia
Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Enrollment
227
Locations
1
Primary Endpoint
Description of the clinical evolution of the patient
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The goal of this observational study is to analyze the data included in the Spanish Registry of Patients with Fanconi anemia to better understand the natural history of the disease, identify genetic risk and prognostic factors, and identify potential therapeutic strategies.

Registry
clinicaltrials.gov
Start Date
May 16, 2024
End Date
June 18, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •All patients in the Spanish Registry of Patients with Fanconi Anemia

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Description of the clinical evolution of the patient

Time Frame: 1 month

Study the clinical evolution of patients with Fanconi anemia

Study Sites (1)

Loading locations...

Similar Trials

Completed
Not Applicable
Evaluation Genotypic, Phenotypic and Prognosis APECED SyndromeAPECED
NCT03751683University Hospital, Lille29
Terminated
Not Applicable
DOAC ADRs Retrospective StudyDrug-Related Side Effects and Adverse Reactions
NCT04247919Cipherome, Inc.3
Recruiting
Not Applicable
Toxicity Genetic Determinants and Response to Azacitidine and Venetoclax in AMLLeukemia, Myeloid, Acute
NCT06580106Wake Forest University Health Sciences50
Completed
Not Applicable
DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients.Death, Sudden, CardiacVentricular FibrillationTachycardiaAtrial FibrillationSick Sinus Syndrome
NCT00478933Medtronic Cardiac Rhythm and Heart Failure1,223
Recruiting
Not Applicable
Observational study on gene mutation and prognosis for patients with resectable pancreatic cancerpancreatic cancer
JPRN-UMIN000032917Kobe university219