Clinical Trials Directory

Trials / Completed

CompletedNCT07135609

Apitoxin Versus Soft Laser for Management of Aphthous Ulceration.

Apitoxin Versus Soft Laser for Management of Aphthous Ulceration

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Tanta University · Academic / Other
Sex
All
Age
15 Years – 40 Years
Healthy volunteers
Not accepted

Summary

The current study evaluated the clinical effect and outcome of locally applied bee venom versus low-level laser therapy (LLLT) for the treatment of recurrent aphthous ulceration.

Detailed description

Recurrent aphthous stomatitis (RAS) is a Painful, idiopathic, and recurrent inflammatory ulceration of the oral cavity. Despite their widespread use, prolonged or frequent application may result in adverse effects such as oral candida. In recent years, low-level laser therapy (LLLT) has gained attention as an alternative treatment for RAS. Apitoxin has been used traditionally to treat a variety of conditions, such as arthritis, rheumatism, back pain, cancer, and skin diseases.

Conditions

Interventions

TypeNameDescription
DEVICELow-level laser therapy (LLLT)Patients managed by Low-level laser therapy (LLLT).
DRUGApitoxinPatients managed with 0.3% Apitoxin Gel.

Timeline

Start date
2024-04-30
Primary completion
2025-02-02
Completion
2025-02-02
First posted
2025-08-22
Last updated
2025-08-22

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07135609. Inclusion in this directory is not an endorsement.