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Clinical Trials/CTRI/2017/04/008386
CTRI/2017/04/008386CompletedPhase 3

Evaluation of efficacy and safety of â??AHPL/AYTOP/2014Aâ?? in patients suffering from aphthous ulcers - an open label, randomized, multi-center, prospective, active controlled, parallel group, clinical study. - NI

Ari Healthcare Pvt Ltd0 sites0 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 3
Status
Completed
Sponsor

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • 1.Patients clinically diagnosed as aphthous ulcers
  • 2.Minor Mouth ulcers that have appeared less than a week prior to the enrollment
  • 3.Ulcers at accessible locations (labial, buccal mucosa, tongue preferably)
  • 4.Who can make all necessary visits and comply with the study procedures
  • 5.Subject willing to participate in clinical trial and who have read, understood and signed informed consent form

Exclusion Criteria

  • 1.Subjects Suffering from any other oral or dental disease or active skin disease.
  • 2.Patient under treatment of ulcers with systemic steroids, vitamins, antibiotics, antihistamines, oral Retinoids or immunomodulatory agents within three months before study entry.
  • 3.Patients having any major systemic diseases including genetic, endocrinal diseases, cancer, HIV, AIDS
  • 4.Known cases of hematological disorders, ulcerative colitis or Crohns disease.
  • 5.Patient who had a history of probable sensitivity to any mouthwash or toothpaste
  • 6.Patients having Anemia or known iron, folic acid, Vit. B12 deficiency
  • 7.Patient having addiction of alcohol or smoking or tobacco chewing
  • 8.Pregnant or lactating women
  • 9.Patients having known hypersensitivity to ingredients used in the study drugs

Investigators

Sponsor
Ari Healthcare Pvt Ltd

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