Clinical Trials Directory

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UnknownNCT04317183

Topical Chamomile in Preventing Chemotherapy-induced Oral Mucositis

The Effect of Topical Chamomile in the Prevention of Chemotherapy-induced Oral Mucositis (a Randomized Controlled Clinical Trial)

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
45 (estimated)
Sponsor
Hams Hamed Abdelrahman · Academic / Other
Sex
All
Age
20 Years – 70 Years
Healthy volunteers
Not accepted

Summary

the main aim of this study is to clinically assess the effectiveness of topical chamomile oral gel in the prevention of chemotherapy-induced oral mucositis.

Detailed description

The study was designed as a randomized, controlled, clinical trial. patients who were undergoing to receive chemotherapy were divided into three groups: Group I: was given conventional treatment. Group II: was given topical oral gel of chamomile. Group III: was given topical oral gel of chamomile in combination with the conventional treatment. All patients have clinically evaluated at the start of the chemotherapy and three weeks later for pain and oral mucositis severity.

Conditions

Interventions

TypeNameDescription
DRUGchamomile topical oral gelChemical constituents of chamomile, such as bisabolol, chamazulene, and the flavonoids apigenin and luteolin, possess anti-inflammatory properties.
DRUGMiconazole Topical Geltopical anti fungal agent
DRUGBBC oral sprayTopical anesthetics and anti-inflammatory agent
DRUGOracure gelTopical analgesic gel

Timeline

Start date
2019-05-15
Primary completion
2020-03-15
Completion
2020-03-30
First posted
2020-03-23
Last updated
2020-03-23

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04317183. Inclusion in this directory is not an endorsement.