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Completed

NCT Number: NCT07702474

Efficacy of 5% Chitosan Nanoparticle Paste in the Treatment of Recurrent Aphthous Stomatitis

The purpose of this study is to evaluate the therapeutic clinical efficacy of a synthesized 5 wt.% chitosan nanoparticle paste compared to a standard topical corticosteroid (triamcinolone acetonide 0.1% oral paste) in patients suffering from minor recurrent aphthous stomatitis. The study specifically monitors changes in clinical ulcer diameter and pain reduction.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

About this study

Recurrent aphthous stomatitis (RAS) is a common oral mucosal disease causing significant pain and discomfort. This randomized, active-controlled, single-blind clinical trial investigates a novel mucoadhesive 5 wt.% chitosan nanoparticle paste formulation synthesized via the ionic gelation technique. Eligible patients diagnosed with minor RAS are randomly allocated in a 1:1 ratio to either Group A (active control: triamcinolone acetonide 0.1% oral paste) or Group B (experimental: 5 wt.% chitosan nanoparticle paste). Both groups apply their designated medication topically four times a day using a sterile swab after rinsing and drying the affected area. Treatment is continued until complete healing of the ulcer occurs. Clinical follow-up examinations are performed periodically at days 0, 1, 6, and 10 to measure the clinical ulcer diameter using a Hu-Friedy periodontal probe and to record subjective pain scores via a Visual Analogue Scale (VAS).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients complaining of oral recurrent ulcers with signs of minor recurrent aphthous stomatitis.
  • History of oral recurrent ulcers with a recurrence rate of 2 to 3 times per year.
  • Ulcer diameter less than 1 cm at baseline.
  • Maximum of 4 days passed since the emergence of the current ulcer.
  • No use of any prior medications or treatment for the current ulcer.
  • Signed written informed consent.

Exclusion criteria

  • Background of systemic diseases, including diabetes mellitus.
  • Connective tissue diseases such as Lupus.
  • Syndromes or diseases related to aphthous ulcers, such as cyclic neutropenia and Behcet's disease.

Treatment and study plan

Triamcinolone Acetonide 0.1% Oral Paste

Drug

Standard reference topical corticosteroid ointment utilized as the active standard of care control.

Other names: Adcortyl

5 wt.% Chitosan Nanoparticle Paste

Drug

Synthesized via ionic gelation method using low molecular weight chitosan and sodium tripolyphosphate, formulated into a 5 wt.% mucoadhesive paste.

Other names: Chitosan Paste, CN

Primary outcomes

  1. Change in clinical ulcer diameter

    Time frame: Days 0, 1, 6, and 10

    Measured in millimeters using a Hu-Friedy periodontal probe to evaluate clinical wound contraction and reduction in lesion size.

Secondary outcomes

  1. Change in pain severity score

    Time frame: Days 0, 1, 6, and 10

    Subjective pain intensity recorded by patients using a Visual Analogue Scale (VAS) graded from 0 (no pain) to 10 (highest rate of pain).

Sponsors and collaborators

Lead sponsor

Kerman University of Medical Sciences

Other

Registry information

Official study title

Wound Healing Effect of Chitosan Nanoparticles and Low Molecular Weight Chitosan: Animal and Clinical Studies

Important dates

Study start
2009
Primary completion
2009
Study completion
2009
First posted
Jul 14, 2026
Registry last updated
Jul 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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