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Topical Mebo Versus Lidocane in Healing Time of Traumatic Oral Ulcer

O

October 6 University

Status

Completed

Conditions

Mebo
Lidocaine
Traumatic Oral Ulceration
Healing

Treatments

Drug: MEBO
Drug: Lidocaine

Study type

Interventional

Funder types

Other

Identifiers

NCT06184282
RECO6U/15-2023

Details and patient eligibility

About

This study aims to assess topical MEBO application on pain relief and wound healing.

Full description

One of the conditions that affect the mouth frequently is a traumatic ulcer. Between 3 and 24 % of the population are affected, which is a significant prevalence. It is symptomatic to treat traumatized ulcers. Oral wound healing is a dynamic process and complicated phenomenon involving secondary concerns, a succession of overlapping stages of rebuilding cell and tissue structure.

Inflammation, granulation tissue creation, matrix formation, re-epithelialization, and tissue remodeling are some of the cellular and physiological activities that occur during wound healing.

Oral wound healing is a dynamic process and complex phenomenon involving secondary issues, series overlapping stages of restoring tissue and cellular structures.

Since 1995, the Moist Exposed Burn Ointment (MEBO), a Chinese burn ointment, has had a recognized US patent. Beta-sitosterol, Phellodendron amurense, Scutellaria baicalensis, Coptis chinensis, Pheretima aspergillum, Beeswax, and sesame oil are all natural ingredients found in MEBO, a pure herbal extract.

Enrollment

28 patients

Sex

All

Ages

20 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age from 20 to 50 years.
  • Both sexes.
  • Systemically healthy patients.
  • Patients with good oral hygiene.

Exclusion criteria

  • Patients with any uncontrolled local or systemic disease.
  • Smokers.
  • Pregnancy and lactation.
  • Patients allergic to the used agents.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

28 participants in 2 patient groups

MEBO group
Experimental group
Description:
MEBO (Julphar®, Ras Al Khaimah, United Arab Emirates) was applied using sterile plastic brush daily and the patients were recalled at 2, 5 and 10 days for evaluating the healing of the ulcer.
Treatment:
Drug: MEBO
Control Group
Active Comparator group
Description:
Lidocaine gel was applied using sterile plastic brush daily and the patients were recalled at 2, 5 and 10 days for evaluating the healing of the ulcer.
Treatment:
Drug: Lidocaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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