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Status unknownNCT00737854TOLPUpdated Dec 11, 2008

Free Soft Tissue Graft in Treatment of Oral Lichen Planus

A Phase 1 interventional study of Surgical resection in Oral Lichen Planus, sponsored by Qazvin University Of Medical Sciences. Status unknown at 1 site in Iran, Islamic Republic of. Open to participants aged 40 Years to 70 Years. Per ClinicalTrials.gov, last updated 2008-12-11.

Sponsored by Qazvin University Of Medical Sciences · Phase 1, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Aug 2008), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 1
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
40 Years to 70 Years
Sex
All
01

Study summary

Oral lichen planus is a common chronic mucocutaneous disease with various clinical forms. Erosive-ulcerative forms usually cause symptoms of pain and discomfort. The most important complication of OLP is development of oral squamous cell carcinoma, although this is a very controversial matter. various treatments have been suggested for OLP but their results are unsatisfactory. Through the experiences of the investigators, corticosteroids (in any form)is not a wise option for treating OLP and has many side effects . More over, immunosuppressive therapy did not influence the risk for oral cancer. The purpose of the study is to determine the efficacy of free soft tissue graft in the treatment of precancerous and symptomatic lesions of OLP. Removal of the lesions up to submucosa has been done. The graft sliced from healthy mucosa also up to submucosa. Then graft will be sutured in position.

According to other authors, basal epithelial layers of the graft remain intact and represent the focus of re-epithelization. New epithelial cells migrate over the basal membrane and appear to guide it by proliferation, will generate new epithelium. The wound is re-epithelialized by proliferation of surrounding healthy epithelial cell, therefore, not contaminated by modified antigens of the cell membrane that are theoretically responsible for lymphocyte aggression. The healthy graft remains free of lesions and appears clinically healthy.

Read the detailed description

Oral lesions in OLP are chronic ,rarely undergo spontaneous remission, are potentially premalignant and are often a source of morbidity. recent study does not support that non reticular OLP are more predisposed to malignant change. Moreover , immunosuppressive therapy did not influence the risk for oral cancer. in general ,all treatment should be aimed at eliminating precancerous lesions ,alleviating symptoms ,and potentially decreasing the risk of malignant transformation. Although the cause of OLP is unknown , it is generally considered to be an immunologically mediated process that microscopically resembles a hypersensitivity reaction .it is characterized by an intense T cell infiltrate localized to epithelium-connective tissue interface. the purpose of the study is to determined the efficacy of free soft tissue graft in treatment of precancerous and symptomatic lesions of OLP. so removal of the lesions up to submucosa will be done. the graft sliced from healthy mucosa also up to submucosa . then graft will be sutured in position.

According to other authors, basal epithelial layers of the graft remain intact and represent the focus of reepithelialization. new epithelial cell migrate over the basal membrane and appear to guide it and by proliferation ,will generate new epithelium. so the wound is re-epithelialized by proliferation of surrounding healthy epithelial cell, therefore, not contaminated by modified antigens of the cell membrane that are theoretically responsible for lymphocyte aggression so the healthy graft remains free of lesions and appears clinically healthy.

02

Conditions studied

  • Oral Lichen Planus

Keywords

  • OLP
  • Free Soft Tissue Graft
  • Treatment
03

In context

Lichen Planus, Oral

139 studies on the registry are indexed under Lichen Planus, Oral; 24 are open to participants now.

This study's planned enrollment of 20 is below the median of 36 across 101 interventional studies indexed under Lichen Planus, Oral.

Browse Lichen Planus, Oral studies →

Lead sponsor

Qazvin University Of Medical Sciences is the lead sponsor of 32 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Biopsy confirmed symptomatic oral lichen planus: WHO histological criteria in combination with clinical appearance will be used for diagnosis
  • Previous routine treatment modalities has been attempted including steroids and immunomodulatory or antioxidant agents. i.e patients who had resistant lesions to routine treatment .removal of possible triggering drugs was also considered.
  • Patients of both sexes between 40 to 70 year's old
  • Patients who have symptoms such as burning sensation, pain
  • Patients who have localized precancerous lesions such as atrophic-erosive/plaque like lichen planus with diameter lesser than 2 cm
  • Patients who agree to this treatment
  • Patients who are willing for evaluation in first week after surgery and every two month for 1 years
  • Patients who agree to final punch biopsy for histopathologic evaluation

Exclusion criteria

Exclusion criteria:

  • Patients who unable to undergo oral surgery
  • Patients suffering from any localized or systemic disease
  • Pregnant patients
  • Smokers
  • Patients who can not continue the study for private or social reasons
  • Patients with generalized oral lichen planus
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
Single (Investigator)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    1 ARM

    Otherwise healthy patients with oral lichen planus (precancerous/erosive OLP)

    Procedure: Surgical resection

Interventions

  • ProcedureSurgical resection

    20 patients with OLP will be selected for this study. Before this routine treatment modalities had been attempted. Removal of possible triggering drug was also considered. Local ethical committee approval will be obtained before the trial starts. Surgical procedure includes: removal of the tissue up to submucosa (containing antigenic properties that caused OLP). A specimen will be sent for histopathologic analysis. The graft sliced from healthy mucosa also up to submucosa. Then the graft trimmed on a gauze soaked in saline and adapted to recipient site. The graft was sutured in position. Checking will be done after 1 week and every two months up to 1 year. Punch biopsy will be done in 1 year after surgery for histopathologic investigations.

    Also known as: surgical resection of OLP

06

What researchers measure

Primary outcomes

  1. Relief of sign & symptoms (every 2 month up to 1 years)

    Time frame: 1 year

Secondary outcomes

  1. Relief of sign & symptoms and no positive histopathologic features of OLP

    Time frame: (time frame 1 years)

07

Study locations

1 of 1 sites recruiting
  • Qazvin University of Medical Sciences
    Qazvin, Qazvin State 3415759811, Iran, Islamic Republic of
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 11, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00737854
Lead sponsor
Qazvin University Of Medical Sciences
First posted
Aug 20, 2008
Start date
May 2008
Primary completion
May 2010 (estimated)
Completion
Dec 2010 (estimated)
Last update
Dec 11, 2008

Study contacts

Farshid - Rayati, DDS
Contact
farshidrayati@yahoo.com
Farshid Rayati, DDS
study director · Qazvin University Of Medical Sciences
Tuba(Aida) Karagah, DDS
principal investigator · QUMS
Farshid Rayati, DDS
study chair · QUMS
Saeid Asefzadeh, PHD
study chair · QUMS
Poopak masumi, DDS-MS
study director · QUMS
pourya falah, student
principal investigator · QUMS

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2008. You cannot join it, but the record below documents what was studied.

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