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Matrix Metalloproteinases Neutralizing Agents in Oral Lichen Planus

Effectiveness of Matrix Metalloproteinase Neutralizing Agent in Treatment of Oral Lichen Planus: A Pilot Study

Status
UNKNOWN
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04336488
Enrollment
40
Registered
2020-04-07
Start date
2020-01-01
Completion date
2020-07-01
Last updated
2020-06-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oral Lichen Planus

Keywords

matrix metalloproteinase inhibitors, orochem, OLP

Brief summary

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

Detailed 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.

Interventions

DRUGMatrix Metalloproteinase Inhibitors (Orochem)

topical application of MMP inhibitors for 3 weeks to evaluate its effectiveness in treating oral lichen planus

DRUGKenacort A,

topical application of both drugs 3 times daily for 3 weeks as an active control

Sponsors

Jaylane kadry Ghonima
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

participant, investigator as well as outcome assessor are blinded

Intervention model description

double equal arms

Eligibility

Sex/Gender
ALL
Age
25 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
change in disease severity scorechange in disease severity score from baseline to 3 weeksThongprasom disease severity score (5-0)

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026