MedPath

Turmeric Oral Rinse in Oral Mucositis

Phase 3
Completed
Conditions
Health Condition 1: null- Subjects with head and neck cancer scheduled to receive chemotherapy or radiotherapy asstandard care and with history or prone todevelop oral mucositis during cancer chemotherapy or radiotherapy
Registration Number
CTRI/2018/05/013936
Lead Sponsor
The Himalaya Drug Company
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

1 Subjects with confirmed histopathologically with head and neck cancer (according to TNM classification) preferably oropharyngeal scheduled to receive chemotherapy or radiotherapy as a standard care.

2 Subjects with history or prone to develop oral mucositis during cancer chemotherapy or radiotherapy.

3 Subjects aged >18 years of either the sex.

4 Subjects willing to give a written informed consent and follow the schedule of the study as per the protocol.

Exclusion Criteria

1 Has participated in a similar clinical investigation in the past four weeks.

2 Severe uncontrolled systemic disorders, diabetes, Hypertension, or genetic and endocrinal disorders.

3 Has used a similar product in the past four weeks.

4 Subjects who refused to sign informed consent.

5 Pregnant and lactating women.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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