Status:
COMPLETED
Cox-2 Inhibition in Radiation-induced Oral Mucositis
Lead Sponsor:
UConn Health
Collaborating Sponsors:
National Institute of Dental and Craniofacial Research (NIDCR)
Pfizer
Conditions:
Oral Mucositis
Eligibility:
All Genders
18-75 years
Phase:
PHASE2
Brief Summary
Oral mucositis refers to ulcerative lesions of the oral mucosa that occur due to radiation therapy given for treatment of head and neck cancer. These lesions are painful, compromise nutrition and qual...
Eligibility Criteria
Inclusion
- Key
- Patients who will be receiving at least 5000 centigray (cGy) radiation therapy to at least 2 of 14 pre-defined areas in the oral cavity.
- Women of childbearing potential must agree to use a medically accepted form of contraception during the course of the study. Women of childbearing potential must have a documented negative pregnancy test within fourteen days of enrollment in the study.
- Patient's willing and able to provide written informed consent for the study.
- Key
Exclusion
- Patients with known hypersensitivity to celecoxib or other COX-2 inhibitors.
- Patients who have experienced asthma, urticaria, or allergic-type reactions after taking salicylates (e.g. aspirin) or Non-steroidal anti-inflammatory drugs (NSAIDs).
- Patients who have demonstrated allergic-type reactions to sulfonamides.
- Patients with a history of gastric, esophageal, pyloric channel or duodenal ulcer disease or gastrointestinal bleeding.
- Patients with a history of inflammatory bowel disease (e.g. Crohn's disease, ulcerative colitis) or pancreatic disease.
- Patients with severe hepatic impairment.
- Patients with advanced renal disease.
- Patients with a significant bleeding disorder.
- Patients under the age of 18 or over the age of 75.
- Women who are pregnant or nursing.
- Patients with a history of thromboembolic events including myocardial infarction, pulmonary embolism, deep venous thrombosis, transient ischemic attack and ischemic cerebrovascular accident (stroke).
- Patients who have had coronary angioplasty, coronary artery bypass surgery or another cardiac revascularization procedure.
- Patients with a history of a cardiac arrhythmia requiring anti-arrhythmic therapy, angina pectoris or congestive heart failure.
Key Trial Info
Start Date :
July 1 2003
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2013
Estimated Enrollment :
43 Patients enrolled
Trial Details
Trial ID
NCT00698204
Start Date
July 1 2003
End Date
December 1 2013
Last Update
June 5 2014
Active Locations (2)
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1
University of Connecticut Health Center
Farmington, Connecticut, United States, 06030-1605
2
Hartford Hospital
Hartford, Connecticut, United States, 06102