RecruitingPhase 2NCT01898416
Safety and Efficacy Study Using 5-ALA Oral Administration as an Adjuvant Therapy on the Rate of Local Tumor Recurrence in Patients Who Have Desmoids Tumors
Studying Desmoid tumor
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
- michal roll
- Principal Investigator
- Jacob Bickels, MD/PhDTel-Aviv Sourasky Medical Center
- Intervention
- 5-AMINOLEVULINIC ACID (5-ALA), is a non fluorescent prodrug.(drug)
- Enrollment
- 140 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2013 – 2026
Study locations (2)
- Tel Aviv sourasky medical center, Tel Aviv, Israel, Israel
- The Aviv Sourasky Medical Center, Tel Aviv, Israel, Israel
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 NCT01898416 on ClinicalTrials.govOther trials for Desmoid tumor
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