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Evaluating effects of Sodium Hyaluronate and four amino acids in oral mucositis preventio

Phase 3
Conditions
oral mucositis.
Oral mucositis (ulcerative), unspecified
K12.30
Registration Number
IRCT20190917044805N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
60
Inclusion Criteria

Age below 18 years old
Undergoing allogenic hematopeitic stem cell transplantation

Exclusion Criteria

Patients with active oral mucositis at the time of admission
History of hypersensitivity reactions to mucosamine spray or any of its ingreedients
Patients with the diagnosis of fanconie's anemia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Oral mucositis severity. Timepoint: every other day, since the day of admission till the day of discharge. Method of measurement: National Cancer Institute Common Terminology of Adverse Events criteria version 5.
Secondary Outcome Measures
NameTimeMethod
Mucositis incidence. Timepoint: Every other day. Method of measurement: Observation.
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