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Effect of Oral Zinc Supplementation as an Adjuvant to Topical Corticosteroid in Oral Lichen Planus Patients

Primary Purpose

Oral Lichen Planus

Status
Unknown status
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
Oral Zinc supplementation
Oral placebo supplementation
Sponsored by
Postgraduate Institute of Dental Sciences Rohtak
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Oral Lichen Planus

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Clinically and histopathologically proven cases of erosive and atrophic OLP.
  2. Patients who are willing to participate in the study.

Exclusion Criteria:

  1. Patients with reticular form of OLP and OLP with muco-cutaneous involvement.
  2. Patients consuming drugs for the treatment of OLP in the past 6 months.
  3. Suspected lichenoid reaction associated with drugs and restorations.
  4. Patients whose histopathological findings indicate moderate to severe dysplasia.
  5. Patients with acquired and congenital immuno-deficiency disorders like AIDS, chemotherapy, addiction to injectable opioids like hemophilia and blood dialysis. These patients are excluded because of difficulty in their biopsy procedure, control of infection, possible interaction with clinical findings of OLP, and their potential doubtful cooperation.
  6. Patients with systemic diseases involving the gastro-intestinal tract.
  7. Known cases of Acrodermatitis enteropathica where difficulty in zinc absorption persists.
  8. Presence of factors that can alter the absorption of zinc like consumption of calcium tablets, iron supplements and high protein diet.
  9. Pregnancy and lactation phase
  10. Alcoholic patients, since alcoholism results in intracellular zinc deficiency.
  11. Recorded allergy to zinc and/or corticosteroids.

Sites / Locations

  • Post Graduate Institute of Dental SciencesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Test group

Control group

Arm Description

The patients will be administered Zinc Acetate tablets (equivalent to 30 mg of elemental zinc/day) for 6 weeks from the baseline. Topical corticosteroid paste will be prescribed according to the intensity of the lesion.

The patients will be administered Placebo tablets for 6 weeks from the baseline. Topical corticosteroid paste will be prescribed according to the intensity of the lesion.

Outcomes

Primary Outcome Measures

Assessment of changes in size of the lesion
Thongprasom score (TS) will be used to assess changes in the size of the lesion. Digital Vernier callipers will be used to measure the largest dimension of ulcers at baseline and at each follow-up visit.
Assessment of changes in pain and burning sensation of the lesion.
Visual Analogue Scale (VAS) will be used to assess changes in pain and burning sensation of the lesion.
Assessment of changes in changes in erythema and ulceration.
Modified Oral Mucositis Index (MOMI)- will be used to assess changes in erythema and ulceration.
Assessment of quality of life of the patient.
Oral Health Impact Profile -14 index (OHIP-14) will be used to assess the quality of life of the patient.

Secondary Outcome Measures

Number of episodes of new lesions in the follow-up period.
The frequency of episodes of new lesions in the follow-up period will be assessed by visual examination
Adverse effects of oral zinc supplementation.
The will adverse effects of oral zinc supplementation.be assessed by interviewing the patients
Requirement for additional systemic steroid therapy.
The requirement for additional systemic steroid therapy will be decided by the presence of non-healing ulcers with persistent VAS scores

Full Information

First Posted
February 18, 2020
Last Updated
July 18, 2020
Sponsor
Postgraduate Institute of Dental Sciences Rohtak
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1. Study Identification

Unique Protocol Identification Number
NCT04278599
Brief Title
Effect of Oral Zinc Supplementation as an Adjuvant to Topical Corticosteroid in Oral Lichen Planus Patients
Official Title
Comparative Evaluation of Effect of Oral Zinc Supplementation and Placebo as an Adjuvant to Topical Corticosteroid Therapy in Oral Lichen Planus Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 15, 2020 (Actual)
Primary Completion Date
September 30, 2020 (Anticipated)
Study Completion Date
September 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Postgraduate Institute of Dental Sciences Rohtak

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Lichen planus is an auto-immune, chronic inflammatory disease that affects mucosal and cutaneous tissue. Erosive and atrophic oral lichen planus (OLP) are difficult to manage because patients present with symptoms ranging from episodic pain to severe discomfort and they have the highest malignant transformation rate (MTR) amongst all the forms of OLP. Zinc is associated with regeneration of epithelium, wound healing and mediating T-lymphocyte function; all of which can lead to healing and re-epithelisation in the lesions of erosive OLP. Besides this, it also has anti-oxidant and anti-inflammatory properties, which lead to decrease in apoptosis and transformation into a malignant state. This study intends to evaluate the effect of oral zinc supplements as an adjuvant to the topical corticosteroid therapy in the treatment of OLP.
Detailed Description
Lichen planus is a chronic muco-cutaneous disorder of the stratified squamous epithelium that affects the oral and genital mucous membrane, skin, hair, nails and scalp.OLP is the mucosal counterpart of cutaneous lichen planus.The disease was first described by Erasmus Wilson in 1866. The prevelance of disease in the Indian sub-continent is about 2.6%,with the mean age being 30-60 years and with a female predilection. The cutaneous form is more persistent and resistant to treatment while OLP is more frequent in occurrence. OLP is a potentially pre-malignant oral epithelial lesion. It is a T-cell mediated auto-immune disease in which the auto-cytotoxic CD8 + T cells trigger the apoptosis of the basal cells of oral epithelium.OLP is an idiopathic disease, although there are certain precipitating factors like HLA-A3, anxiety & stress, diabetes and hypertension. OLP occurs bilaterally, the most common sites being buccal mucosa, tongue, lips, gingiva, floor of mouth and palate. Wickham's striae are a pathogonomic feature. It has six clinical presentations- Reticular, Erosive, Atrophic, Plaque-like, Papular and Bullous.The reticular form is most common but its asymptomatic, while the erosive form is most severe with symptoms ranging from mild burning to severe pain. The range of MTR for OLP is about 0-5%, with the highest rate for erosive and atrophic types.Erosive OLP lesions arise as a complication of the atrophic process after trauma or ulceration. Appear as a central area of erosion with yellowish fibrinous exudate surrounded by erythema, with Wickham's striae in the periphery. Atrophic OLP lesions appear bright red due to loss of epithelium. A review study done on the recent concepts in the treatment of OLP concluded that corticosteroids (mostly topical, rarely systemic) continue to be the mainstay of management of OLP. However, there are some other drugs which have a significant contribution such as- Calcineurin inhibitors (cyclosporine, tacrolimus, pimecrolimus), Retinoids, Dapsone, Hydroxychloroquine, Mycophenolate mofetil and Enoxaprin. The non-pharmacological treatment modalities include PUVA therapy, photodynamic therapy and laser therapy. A recently conducted study found out that serum zinc levels were significantly decreased in patients with erosive OLP in comparison with patients of non-erosive OLP, which may be responsible for disintegration of epithelium in erosive OLP lesions. The association of OLP and zinc lies in the fact that zinc is associated with the regeneration of epithelium, enhancement of enzyme activity, contributes to protein structure, helps in wound healing as well as inhibition and stimulation of lymphocyte reaction.The deficiency of zinc also leads to compromised T-cell mediated immune defence.Zinc also has anti-oxidant and anti-inflammatory properties, which can decrease apoptosis and transformation to a malignant state. Thus, the present study intends to evaluate the role of oral zinc supplementation as an adjuvant to topical corticosteroid therapy on the treatment of oral lichen planus.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oral Lichen Planus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
42 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Test group
Arm Type
Experimental
Arm Description
The patients will be administered Zinc Acetate tablets (equivalent to 30 mg of elemental zinc/day) for 6 weeks from the baseline. Topical corticosteroid paste will be prescribed according to the intensity of the lesion.
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
The patients will be administered Placebo tablets for 6 weeks from the baseline. Topical corticosteroid paste will be prescribed according to the intensity of the lesion.
Intervention Type
Drug
Intervention Name(s)
Oral Zinc supplementation
Other Intervention Name(s)
Zinc Acetate
Intervention Description
In the test group, the patients will be administered Zinc Acetate tablets (equivalent to 30 mg of elemental zinc/day) for 6 weeks from the baseline. They will also be will be administered, topical corticosteroid paste- Triamcinolone acetonide- 0.1%, to be applied thrice a day till the lesions disappeared and the dosage will be tapered accordingly.The patients will be instructed to take the tablets and apply the paste after meals.The patients will be kept on a monthly follow-up for 3 months.
Intervention Type
Drug
Intervention Name(s)
Oral placebo supplementation
Other Intervention Name(s)
Placebo
Intervention Description
In the control group, the patients will be administered Placebo tablets for 6 weeks from the baseline. They will also be administered, topical corticosteroid paste- Triamcinolone acetonide- 0.1%, to be applied thrice a day till the lesions disappeared and the dosage will be tapered accordingly.The patients will be instructed to take the tablets and apply the paste after meals.The patients will be kept on a monthly follow-up for 3 months.
Primary Outcome Measure Information:
Title
Assessment of changes in size of the lesion
Description
Thongprasom score (TS) will be used to assess changes in the size of the lesion. Digital Vernier callipers will be used to measure the largest dimension of ulcers at baseline and at each follow-up visit.
Time Frame
Baseline, 6 weeks and 3 months.
Title
Assessment of changes in pain and burning sensation of the lesion.
Description
Visual Analogue Scale (VAS) will be used to assess changes in pain and burning sensation of the lesion.
Time Frame
Baseline, 6 weeks and 3 months
Title
Assessment of changes in changes in erythema and ulceration.
Description
Modified Oral Mucositis Index (MOMI)- will be used to assess changes in erythema and ulceration.
Time Frame
Baseline, 6 weeks and 3 months
Title
Assessment of quality of life of the patient.
Description
Oral Health Impact Profile -14 index (OHIP-14) will be used to assess the quality of life of the patient.
Time Frame
Baseline, 6 weeks and 3 months
Secondary Outcome Measure Information:
Title
Number of episodes of new lesions in the follow-up period.
Description
The frequency of episodes of new lesions in the follow-up period will be assessed by visual examination
Time Frame
Baseline, 6 weeks and 3 months
Title
Adverse effects of oral zinc supplementation.
Description
The will adverse effects of oral zinc supplementation.be assessed by interviewing the patients
Time Frame
Baseline, 6 weeks and 3 months
Title
Requirement for additional systemic steroid therapy.
Description
The requirement for additional systemic steroid therapy will be decided by the presence of non-healing ulcers with persistent VAS scores
Time Frame
Baseline, 6 weeks and 3 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Clinically and histopathologically proven cases of erosive and atrophic OLP. Patients who are willing to participate in the study. Exclusion Criteria: Patients with reticular form of OLP and OLP with muco-cutaneous involvement. Patients consuming drugs for the treatment of OLP in the past 6 months. Suspected lichenoid reaction associated with drugs and restorations. Patients whose histopathological findings indicate moderate to severe dysplasia. Patients with acquired and congenital immuno-deficiency disorders like AIDS, chemotherapy, addiction to injectable opioids like hemophilia and blood dialysis. These patients are excluded because of difficulty in their biopsy procedure, control of infection, possible interaction with clinical findings of OLP, and their potential doubtful cooperation. Patients with systemic diseases involving the gastro-intestinal tract. Known cases of Acrodermatitis enteropathica where difficulty in zinc absorption persists. Presence of factors that can alter the absorption of zinc like consumption of calcium tablets, iron supplements and high protein diet. Pregnancy and lactation phase Alcoholic patients, since alcoholism results in intracellular zinc deficiency. Recorded allergy to zinc and/or corticosteroids.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sanjay Tewari
Phone
01262283876
Email
principalpgidsrohtak@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shagun Solanki
Organizational Affiliation
Post Graduate Institute of Dental Sciences, Rohtak
Official's Role
Principal Investigator
Facility Information:
Facility Name
Post Graduate Institute of Dental Sciences
City
Rohtak
State/Province
Haryana
ZIP/Postal Code
124001
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sanjay TEWARI
Phone
01262283876
Email
principalpgids@yahoo.in

12. IPD Sharing Statement

Learn more about this trial

Effect of Oral Zinc Supplementation as an Adjuvant to Topical Corticosteroid in Oral Lichen Planus Patients

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