CompletedPhase 2NCT02080624
Efficacy and Safety Study of Topical Rapamycin Associated With Pulsed Dye Laser in Patients With Sturge-Weber Syndrome
Studying Sturge-Weber syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Clinica Universidad de Navarra, Universidad de Navarra
- Principal Investigator
- Maider Pretel, MD PhDClinica Universidad de Navarra
- Intervention
- Drug: Topical Rapamycin(drug)
- Enrollment
- 23 enrolled
- Eligibility
- 16-65 years · All sexes
- Timeline
- 2011 – 2012
Study locations (1)
- Clinica Universidad de Navarra, Pamplona, Navarre, Spain
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT02080624 on ClinicalTrials.govOther trials for Sturge-Weber syndrome
Additional recruiting or active studies for the same condition.
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- ACTIVE NOT RECRUITINGNANCT04517565Longitudinal Neuroimaging in Sturge-Weber SyndromeWayne State University
- ACTIVE NOT RECRUITINGNCT01425944Innovative Approaches to Gauge Progression of Sturge-Weber SyndromeHugo W. Moser Research Institute at Kennedy Krieger, Inc.