Chemoprevention of Oral Premalignant Lesions
Completed · Phase 2
Conditions studied: Precancerous Conditions
In brief
Reduction in size and number of oral premalignant lesions
Key facts
- Study ID
- NCT00036283
- Run by
- Pfizer
- People needed
- 42
- Starts
- 2000-11-01
- Expected to finish
- 2004-04-01
- Last updated by the study team
- 2008-09-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 8mm oral premalignant lesion that has not been biopsied in the past 6 months
You may not qualify if…
- Taking >100mg daily dose of NSAIDS (Non-steroidal anti-inflammatory drugs)
Where it is running
- Pfizer Investigational Site — Farmington, Connecticut, United States
- Pfizer Investigational Site — Shreveport, Louisiana, United States
- Pfizer Investigational Site — Ann Arbor, Michigan, United States
- Pfizer Investigational Site — Minneapolis, Minnesota, United States
- Pfizer Investigational Site — New York, New York, United States
- Pfizer Investigational Site — Houston, Texas, United States
- Pfizer Investigational Site — Seattle, Washington, United States
Full record on ClinicalTrials.gov
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