Actively Recruiting

Phase 2
Phase 3
Age: 35Years - 60Years
All Genders
NCT06988527

Treatment Outcomes and Patient Satisfaction of Oral Lichen Planus Treatment

Led by Dar Al Uloom University · Updated on 2026-02-17

56

Participants Needed

1

Research Sites

58 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to assess Honey in orabase (1:1) for treating patients with OLP and improving their quality of life: The research question aims to answer: Does honey in orabase (1:1) improve or reduce OLP symptoms compared to the standardized treatment by triamcinolone acetonide 0.1% drug and improve the patient's quality of life? Participants will: Take drug ABC or a placebo every day for 4 months Visit the clinic once every 2 weeks for checkups and tests Keep a diary of their symptoms and the number of times they use a rescue inhaler

CONDITIONS

Official Title

Treatment Outcomes and Patient Satisfaction of Oral Lichen Planus Treatment

Who Can Participate

Age: 35Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with a clinical diagnosis of oral lichen planus
  • Symptomatic OLP lesions (erosive or atrophic)
  • Participants aged between 35 and 60 years
  • Able to adhere to the study protocol
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Patients with other oral mucosal disorders or systemic conditions affecting OLP or wound healing
  • Allergies or hypersensitivity to honey or triamcinolone
  • Use of systemic corticosteroids or immunosuppressive agents
  • Pregnant or lactating women
  • Inability to understand or follow study instructions
  • Unable to provide informed written consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Dar AlUloom University

Riyadh, Saudi Arabia, 11512

Actively Recruiting

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Research Team

S

Sally A ElHaddad, Assist Prof

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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