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Propolis in Primary Herpetic Gingivostomatitis

NCT06778655 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-01-30

No results posted yet for this study

Summary

The purpose of the present study is to investigate the efficacy of 5% propolis gel in the treatment of primary herpetic gingivostomatitis in children and its effect on salivary IFN-γ levels.

Conditions

  • Herpetic Gingivostomatitis

Interventions

DIETARY_SUPPLEMENT

5% propolis gel

5% propolis gel (prepared according to Joshy et al. 2018) Joshy A, Doggalli N, Patil K, Kulkarni PK. To Evaluate the Efficacy of Topical Propolis in the Management of Symptomatic Oral Lichen Planus: A Randomized Controlled Trial. Contemp Clin Dent. 2018 Jan-Mar;9(1):65-71.

OTHER

Placebo gel

placebo mucoadhesive gel having the same flavor, consistency, and color as the propolis.

Sponsors & Collaborators

  • Fayoum University

    lead OTHER

Principal Investigators

  • Rania Shalaby, associate professor · Fayoum University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
3 Years
Max Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-10
Primary Completion
2025-01-15
Completion
2025-01-15

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06778655 on ClinicalTrials.gov