At a glance
ClinicalIndex Comparison RecordN/ACompleted· 1,046 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Evaluating Genetic Modifiers of Cutaneous Neurofibromas in Adults With Neurofibromatosis Type 1
In Brief
An observational study for Neurofibromatosis 1. Completed, enrolled 1,046 participants across 2 sites.
Detailed Summary
The main goal of this protocol is to develop a well-phenotyped genetic biobank to identify genetic variants associated with the heterogeneous clinical presentations of Neurofibromatosis Type 1 (NF1). This will allow for improve understanding of NF1 pathogenesis and more personalized disease management. The investigators will conduct a GWAS analysis to identify common genetic risk variants associated with the development of cutaneous neurofibromas.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsNeurofibromatosis 1
CountriesUnited States
Timeline
N/ACompletedFinished
20222023202420252026
Enrollment StartMay 2021
First PostedJun 2021
Primary CompletionSep 2025
Study CompletionNov 2025
TodayJul 2026
First PostedJun 28, 2021
Enrollment StartMay 7, 2021
Primary CompletionSep 30, 2025
Study CompletionNov 24, 2025
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 5.0 years ago