Trial Information
Effect of Quercetin in Prevention and Treatment of Chemotherapy Induced Oral Mucositis in Blood Dyscrasias
Inclusion Criteria:
- patient under chemotherapy
- for a hematologic malignancy
- the hematologist permits the trial on the patient
- agreement of patient for participating in the trial
Exclusion Criteria:
- presence pf ANY oral lesion at the beginning of the trial
- loss of follow up
- use of digoxin and cyclosporine
- patient death
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Outcome Measure:
lower grade of mucositis
Outcome Description:
grade of mucositis due to WHO criteria
Outcome Time Frame:
3 weeks
Safety Issue:
No
Principal Investigator
Pegah Mosannen Mozafari, assistant professor
Investigator Role:
Study Director
Investigator Affiliation:
Mashhad University of Medical Sciences
Authority:
Iran: Ministry of Health
Study ID:
89470
NCT ID:
NCT01732393
Start Date:
January 2010
Completion Date:
January 2012
Related Keywords:
- Chemotherapy Induced Oral Mucositis
- Quercetin
- Chemotherapy
- Mucositis
- Hematologic Malignancies
- Stomatitis
- Mucositis