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Topical Nicotinamide in Treatment of DLE

Primary Purpose

Discoid Lupus Erythematosus

Status
Completed
Phase
Early Phase 1
Locations
Egypt
Study Type
Interventional
Intervention
Nicotinamide Topical
Sponsored by
Al-Azhar University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Discoid Lupus Erythematosus

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age: between 18 years and 65 years old
  • Patients clinically and histopathologically newly diagnosed as DLE
  • Patients clinically and histopathologically diagnosed with cutaneous lupus erythematosus that has not responded to treatment with hydroxychloroquine(200-400mg/day) plus corticosteroid at a dosage less than the equivalent of (0.5mg/kg/day) for the preceding two months or a longer period

Exclusion Criteria:

  • Age < 18 years old
  • Pregnant and lactating women
  • A history of treatments with multivitamins in the recent month
  • Soft tissue infection
  • Severe comorbidities including heart failure, respiratory failure
  • Acute severe infections such as cellulitis or a history of HBV or HCV

Sites / Locations

  • AL-Azhar University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

Topical Nicotinamide 2%

Topical Nicotinamide 4%

Placebo

Arm Description

will receive topical nicotinamide 2%

will receive topical nicotinamide 4%

Subjects will receive only cream/gel base without API for control

Outcomes

Primary Outcome Measures

Severity index
A change in discoid lupus erythematosus severity index
Activity score
A change in discoid lupus erythematosus activity score

Secondary Outcome Measures

Response
defined as > 25% change in activity score at the end of treatment
Remarkable response
defined as > 50% change in activity score
The dermatology life Quality Index score
A change in Dermatology life Quality Index score as it reflects the quality of life related to skin manifestations

Full Information

First Posted
April 26, 2022
Last Updated
October 22, 2022
Sponsor
Al-Azhar University
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1. Study Identification

Unique Protocol Identification Number
NCT05362188
Brief Title
Topical Nicotinamide in Treatment of DLE
Official Title
Efficacy and Safety of Topical Nicotinamide in Treatment of Discoid Lupus Erythematosus
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
March 1, 2022 (Actual)
Primary Completion Date
September 1, 2022 (Actual)
Study Completion Date
September 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Al-Azhar University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Cutaneous lupus erythematosus (CLE) is lupus affecting the skin. In this autoimmune disease, the body's immune system attacks healthy skin. There are 3 main types: Acute cutaneous lupus, Subacute cutaneous lupus, and Chronic cutaneous lupus ("discoid lupus"). Lupus most often appears between the ages of 20 and 50 years; it affects women more than men, and it may happen more in patients with a family history of lupus or other autoimmune diseases.
Detailed Description
DLE is the most common form of chronic cutaneous erythematosus and can occur as a localized form (80%) with lesions on the face, ears, and scalp or as disseminated DLE (20%) with lesions above and below the neck. The disseminated form of DLE, especially when involving the trunk, is associated with an increased risk of progression to SLE. It is unusual for discoid lesions to be present below the neck without lesions also being present above the neck. Occasionally, discoid lesions develop on mucosal surfaces, including the lips, nasal mucosa, conjunctivae, and genital mucosa. Some patients with discoid lesions exhibit a photodistribution. Sun exposure seems to play a role in the development of lesions. For discoid lupus erythematosus without associated SLE (CDLE), the evidence does not show whether circulating inflammatory cells and autoantibodies are involved in the pathogenesis, but it is evident that the cutaneous inflammatory infiltrates are dominated by Th1. The first morphological sign of DLE is a well-defined, annular erythematous patch or plaque of varying size followed by follicular hyperkeratosis, which is adherent to the skin. By removing the adherent scale, follicle-sized keratotic spikes similar to carpet tacks can be seen ("carpet tack sign"). The lesions slowly expand with active inflammation and hyperpigmentation at the periphery leaving depressed central atrophy and scarring, telangiectasia, and hypopigmentation. DLE can progress to irreversible scarring alopecia on the scalp. Although uncommon, a squamous cell carcinoma can develop in a longstanding discoid lesion. A biopsy from the lesion for routine histologic examination is usually diagnostic of DLE. Atrophic epidermis, keratotic plugging of the follicles, hydropic degeneration of the basal cells, and patchy perivascular and perifollicular lymphocytic infiltrate are characteristic. Early treatment of discoid lupus lesions may lead to the total clearing of skin lesions, but treatment failure results in permanent scarring. Hair loss, depressed scars, and pigmentary changes are often disfiguring, particularly in darker-skinned people. Some general measures, such as sun avoidance and liberal application of sunscreen, are encouraged because cutaneous lesions are known to be exacerbated by sunlight. Smoking cessation is encouraged, as this can increase DLE disease activity. While antimalarials such as hydroxychloroquine have been widely used as a first-line treatment for lupus-associated skin lesions, 30% of patients with lupus do not respond to this medication. Other available therapies such as corticosteroids and thalidomide can also be applied, however, their toxic side effects limit their clinical use. Recent studies by the investigators have shown that nicotinamide, a water-soluble vitamin whose side effects are considered minimal, can protect against skin lesions and autoantibody production. Thus it is hypothesized that nicotinamide treatment could be a novel therapy for lupus-associated skin lesions in patients with LE. Nicotinamide is the amide form of vitamin B3 . It is the precursor of numerous reactions in the body including adenosine triphosphate (ATP) production and consequently can be used in many dermatological disorders.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Discoid Lupus Erythematosus

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Topical Nicotinamide 2%
Arm Type
Experimental
Arm Description
will receive topical nicotinamide 2%
Arm Title
Topical Nicotinamide 4%
Arm Type
Experimental
Arm Description
will receive topical nicotinamide 4%
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Subjects will receive only cream/gel base without API for control
Intervention Type
Drug
Intervention Name(s)
Nicotinamide Topical
Other Intervention Name(s)
Topical treatment of skin lesions
Intervention Description
Patients with discoid lupus erythematosus (face & scalp) will be given topical nicotinamide in two concentrations (2&4%) to apply twice daily for 12 consecutive weeks and then follow up. Topical nicotinamide will be prepared in different forms (cream & gel).
Primary Outcome Measure Information:
Title
Severity index
Description
A change in discoid lupus erythematosus severity index
Time Frame
from base line ( visit 0 ) to 1 , 2 respectively
Title
Activity score
Description
A change in discoid lupus erythematosus activity score
Time Frame
from base line ( visit 0 ) to 1 , 2 respectively
Secondary Outcome Measure Information:
Title
Response
Description
defined as > 25% change in activity score at the end of treatment
Time Frame
2 months
Title
Remarkable response
Description
defined as > 50% change in activity score
Time Frame
2 months
Title
The dermatology life Quality Index score
Description
A change in Dermatology life Quality Index score as it reflects the quality of life related to skin manifestations
Time Frame
2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age: between 18 years and 65 years old Patients clinically and histopathologically newly diagnosed as DLE Patients clinically and histopathologically diagnosed with cutaneous lupus erythematosus that has not responded to treatment with hydroxychloroquine(200-400mg/day) plus corticosteroid at a dosage less than the equivalent of (0.5mg/kg/day) for the preceding two months or a longer period Exclusion Criteria: Age < 18 years old Pregnant and lactating women A history of treatments with multivitamins in the recent month Soft tissue infection Severe comorbidities including heart failure, respiratory failure Acute severe infections such as cellulitis or a history of HBV or HCV
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ahmed Hassan Nouh, MD
Organizational Affiliation
Al-Azhar university Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
AL-Azhar University Hospital
City
Cairo
ZIP/Postal Code
11865
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No

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Topical Nicotinamide in Treatment of DLE

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