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Clinical study to check the effectiveness and safety of AphtoFix® Mouth Ulcer Cream in subjects suffering from mouth ulcer.

Phase 4
Completed
Conditions
Health Condition 1: K928- Other specified diseases of the digestive system
Registration Number
CTRI/2014/08/004918
Lead Sponsor
Bonyf AG
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Male or female subjects with 18 â?? 65 years of age (both

inclusive).

2. Subjects having mouth ulcer size >2 mm in locations for easily

accessible for evaluation and treatment.

3. Subject with time of onset of mouth ulceration within 48 hours.

4. Subject who agreed, not to use any other medication to treat

mouth ulcer during study period.

5. Subject willingness to comply with the study schedule and

procedures.

6. Subject / legally acceptable representative (LAR) of subject

willing to sign and date written informed consent to participate

in the study. However, if the subject/LAR of subject is illiterate,

the impartial witness would sign the ICF.

Exclusion Criteria

1. Subjects with a history of allergy for content present in

AphtoFix®

2. Subjects with any invasive dental procedures within 2 weeks

prior to screening visit.

3. History of uncontrolled chronic disease (e.g. chronic liver

disease, chronic renal disease)

4. Use of any other medication to treat mouth ulcer in current

episode.

5. Participation in any other clinical study during last 30 days.

6. Subject with any condition which in the opinion of the

investigator makes the subject unsuitable for inclusion.

7. Subject is a female who is pregnant or willing to get pregnant,

not ready to use contraceptive measures during the trial period,

or is breast feeding.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
- Ulcer size reduction. <br/ ><br>- Reduction in number of ulcers. <br/ ><br>- Pain reduction by assessing pain intensity.Timepoint: 14 days
Secondary Outcome Measures
NameTimeMethod
- Duration of ulcer (Days need for complete healing). <br/ ><br>- Number and frequency of application. <br/ ><br>- Quality of life evaluation using mouth ulcer QOL <br/ ><br>Questionnaire.Timepoint: 14 Days
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