The effect of gel containing Prunella vulgaris extract on labial herpes

Phase 2

• Conditions: recurrent herpes labialis.; Herpesviral vesicular dermatitis

• Registration Number: IRCT2016021412438N16
• Lead Sponsor: Barij Research Center of Medicinal Herbs

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Inclusion: People 18 to 70 years old with recurrent herpes labialis that Less than 12 hours have passed vesicate.
Exclusion criteria: Pregnancy and lactatin; use the antiviral drug in the past two weeks; have a history of immunotherapy in the last year; stimulating the immune system in the last month; Other mucocutaneous disorders; history of RAS ;history of allergy to the plant used in the study of allergic reaction during the study

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Clinical symptoms of blisters. Timepoint: Baseline and End-of-trial. Method of measurement: Observation.;Burning. Timepoint: At days 0, 2, 4, 7. Method of measurement: VAS.;Iitching. Timepoint: At days 0, 2, 4, 7. Method of measurement: VAS.;Soreness. Timepoint: At days 0, 2, 4, 7. Method of measurement: VAS.;Tingling. Timepoint: At days 0,2,4,7. Method of measurement: VAS.