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Matrix Metalloproteinases Neutralizing Agents in Oral Lichen Planus

J

Jaylane kadry Ghonima

Status and phase

Unknown
Early Phase 1

Conditions

Oral Lichen Planus

Treatments

Drug: Kenacort A,
Drug: Matrix Metalloproteinase Inhibitors (Orochem)

Study type

Interventional

Funder types

Other

Identifiers

NCT04336488
MMPs in lichen

Details and patient eligibility

About

The current study will be conducted to evaluate the effectiveness of matrix metalloproteinases inhibitors on erosive oral lichen planus.

Full description

Matrix metalloproteinases inhibitor (Orochem) will be given to patients with Oral erosive lichen planus three times daily for 3 weeks. Then the subjective discomfort and pain severity as well as the objective disease severity scores will be collected.

Enrollment

40 estimated patients

Sex

All

Ages

25+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients diagnosed with erosive OLP confirmed with a biopsy.
  • patients should have symptomatic lesions

Exclusion criteria

  • Patients who were under anticoagulant medications, suffering from any systemic diseases or having any physical or mental abnormality, pregnant and lactating women, smokers.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

40 participants in 2 patient groups

Orochem (Test)
Experimental group
Description:
fifteen patients with lichen planus will be treated with MMPs neutralizing agent 3 times daily for 3 weeks. then pain, discomfort and disease severity will be assessed at 1 and 3 weeks periods.
Treatment:
Drug: Matrix Metalloproteinase Inhibitors (Orochem)
Conventional (Control)
Active Comparator group
Description:
fifteen patients with oral lichen planus confirmed with a biopsy will be treated with topical corticosteroids, topical antifungal 3 timed daily for 3 weeks. then pain, discomfort and disease severity will be assessed at 1 and 3 weeks periods.
Treatment:
Drug: Kenacort A,

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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