Prevention of chemotherapy-induced stomatitis

Phase 2

• Conditions: Chemotherapy-induced mucositis.; Other and unspecified lesions of oral mucosa

• Registration Number: IRCT2012101311099N1
• Lead Sponsor: Vice Chancellor for research of Shahid Sadoghi University of Medical Sciences- Yazd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

Possess one of hematologic malignancies( acute lymphoid leukemia (ALL) or acute myeloid leukemia (AML) according to the oncologist- similar chemotherapy treatment planning- patients are beginning to chemotherapy (new case)- absence of any fungal,viral or other lesions in the patient's mouth

Exclusion criteria:
appearance of fungal or viral lesions in the patient's mouth- lack of patient cooperation protocol X or Y

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Day 0(Concurrent with intervention)-days 6,9,12 and 14 after the start of intervention. Method of measurement: VAS scale.;Erythema. Timepoint: Day 0(Concurrent with intervention)-days 6,9,12 and 14 after the start of intervention. Method of measurement: Square centimeter.;Grading of stomatitis. Timepoint: Day 0(Concurrent with intervention)-days 6,9,12 and 14 after the start of intervention. Method of measurement: WHO grading.;Ulcer. Timepoint: Day 0(Concurrent with intervention)-days 6,9,12and 14 after the start of intervention. Method of measurement: Square centimeter.