Oral Mucositis (Ulcerative) Due to Radiation Clinical Trial
Official title:
The Effectiveness of Melatonin in Prevention of Radiation-induced Oral Mucositis
Verified date | June 2019 |
Source | Alexandria University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main aim of this study was to evaluate the effectiveness of melatonin in prevention of radiation induced oral mucositis clinically and biochemically.
Status | Completed |
Enrollment | 40 |
Est. completion date | December 1, 2018 |
Est. primary completion date | November 9, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 25 Years and older |
Eligibility |
Inclusion Criteria: - Patients who are going to receive radiotherapy as a treatment of head and neck cancer either as postoperative (adjuvant) therapy or definitive therapy. - Patients whose radiotherapy treatment planned dose is between 60-70 Gy. - Patients who had received chemotherapy prior to radiotherapy or are going to receive chemotherapy in concomitant to radiotherapy. Exclusion Criteria: - Patients under Anticoagulants such as warfarin, heparin, or aspirin. - Patients under Fluvoxamine (Luvox) and Nifedipine medications. - Patients whose radiotherapy treatment planned dose is lower than 60 Gy. - Pregnant and lactating women. - Patients suffering from any uncontrolled systemic diseases (such as diabetes, cardiovascular, liver disorder, renal dysfunction) - Patients with findings of any physical or mental abnormality which would interfere with or be affected by the study procedure. |
Country | Name | City | State |
---|---|---|---|
Egypt | Outpatient clinic of Department of Clinical Oncology, Faculty of Medicine, Alexandria University | Alexandria |
Lead Sponsor | Collaborator |
---|---|
Hams Hamed Abdelrahman | Alexandria University |
Egypt,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in severity of oral mucositis at different time points along the study | Oral mucositis will be evaluated by the World Health Organization (WHO) scale which record the extent and severity of oral mucositis at the third and sixth week after the first radiotherapy session. This scale combines both subjective and objective measures of oral mucositis. World Health Organization (WHO) scale for oral mucositis: Grade 0 = No oral mucositis Grade 1 = Erythema and Soreness Grade 2 = Ulcers, able to eat solids Grade 3 = Ulcers, requires liquid diet (due to mucositis) Grade 4 = Ulcers, alimentation not possible (due to mucositis) |
up to 3 and 6 weeks | |
Primary | Changes in the total antioxidant capacity (TAC) in saliva at different time points along the study | TAC is an index that measures total capacity of antioxidants in biological fluids using Colorimetric Method. it can evaluate the antioxidant response against the free radicals produced by radiotherapy. Normal reference values for TAC in saliva: 0.3-1 mM/L Higher values than normal range indicate higher level of TAC Changes in the total antioxidant capacity were evaluated at the first day of radiotherapy session (baseline) and six weeks later |
Baseline (day 0) and up to 6 weeks | |
Secondary | Pain and discomfort severity at different time points along the study: Numeric Rating Scale | Discomfort and pain severity were reported by each patient using Numeric Rating Scale (NRS) at the third and sixth week after the first radiotherapy session. The NRS was calibrated from 0 to 10 with ranges tagged as; No pain (NRS 0) Mild pain (NRS 1-3) Moderate pain (NRS 4-7) Unbearable pain (NRS 8-10) |
up to 3 and 6 weeks |
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