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Zinc Sulfate in the Treatment of Rosacea: A Randomized, Controlled Trial

Primary Purpose

Rosacea

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
zinc sulfate
placebo
Sponsored by
Essentia Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rosacea focused on measuring Rosacea

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosis of facial rosacea made or confirmed by one of the investigators.
  • Severity of signs of rosacea "greater than mild" at the time of enrollment.

Exclusion Criteria:

  • Treatment for rosacea during the 3 months prior to enrollment.
  • Use of zinc dietary supplement > 25 mg per day during the 3 months prior to enrollment ( Most patients taking multivitamins with Zinc, often 15 mg per day, will not be excluded, whereas most patients taking additional Zinc supplements, often 25-50 mg per day or more will be excluded.)
  • Diagnosis of rosacea fulminancy.
  • Pregnant or breast feeding.

Sites / Locations

  • St. Mary's Duluth Clinic Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Zinc sulfate

Lactose

Arm Description

220 mg of zinc sulfate

270 mg lactose

Outcomes

Primary Outcome Measures

Severity of Facial Rosacea After 90 Days of Treatment
Modified Rosacea Severity Scoring System evaluating four signs of rosacea, flushing (transient erythema or redness), erythema (redness), papules and pustules and telangiectasia (spider-veins) ranges from 0 (best, absent) to 12 (worst, severe on all items)

Secondary Outcome Measures

Full Information

First Posted
October 31, 2006
Last Updated
June 3, 2011
Sponsor
Essentia Health
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1. Study Identification

Unique Protocol Identification Number
NCT00395226
Brief Title
Zinc Sulfate in the Treatment of Rosacea: A Randomized, Controlled Trial
Official Title
"Zinc Sulfate in the Treatment of Rosacea: A Randomized, Controlled Trial." Prospective, Double Blind, Randomized, Controlled Trial Comparing the Effects of Supplemental Zinc Sulfate and Placebo on the Severity of Rosacea.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2011
Overall Recruitment Status
Terminated
Why Stopped
Difficulty recruiting subjects
Study Start Date
July 2006 (undefined)
Primary Completion Date
July 2008 (Actual)
Study Completion Date
July 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Essentia Health

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Rosacea is a common chronic dermatological condition, characterized by recurrent or persistent redness, permanent dilation of small blood vessel causing small red lesions, and papules/pustules. The signs of rosacea are usually confined to the face, but may appear on the neck, scalp or trunk. Opthalmologic findings are also common. Rosacea is usually described as being most common in fair skinned women over 40. The purpose of the study is to determine whether oral Zinc Sulfate treatment is an effective treatment for facial rosacea.
Detailed Description
Rosacea is a common chronic dermatological condition. The epidemiology of rosacea has not been determined extensively, due to part in problems with case definition. Rosacea is usually described as being most common in fair skinned women over the age of 40. However it occurs in most adult populations, including both men and women of all ages, and in people of many complexion types, including African Americans and Asians. Although rosacea is encountered frequently in primary care and dermatology practices, its precise incidence and prevalence are not known. The etiology and pathogenesis of rosacea are unknown. Both genetic and environmental factors are thought to be important. A wide range of medical and surgical interventions have been used in the management of rosacea, including dietary management, topical and systemic antibiotics, azelaic acid, low dose isotretinoin, and laser treatments for telangiectasia and rhinophyma. No single regimen has been found to be entirely satisfactory. Zinc has been found to be effective in managing several dermatological conditions, especially acne. It has also been found to be of benefit in dermatological conditions such as viral warts and cutaneous leishmaniasis. No studies have been published on the use of Zinc in the treatment of rosacea. This will be a prospective, double blind, randomized, controlled trial, comparing the effects of supplemental and placebo on the severity of rosacea. Enrolled subjects will be assigned to one of two study arms. Subjects and investigators will be blinded regarding treatment. After evaluation, meeting the study criteria,obtaining informed consent, and initiating study related procedures, the subject will take oral study drug or placebo, bid, for 90 days. Subjects are followed via phone call at one week and 6 weeks after enrollment into the study. At the conclusion of the 90 day study, subjects will be re-examined. The primary endpoint of this study will be the severity of rosacea at the end of the 90 day intervention period. The efficacy of Zinc vs. placebo will be assessed by a comparison of the change in the severity of rosacea.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rosacea
Keywords
Rosacea

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
65 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Zinc sulfate
Arm Type
Experimental
Arm Description
220 mg of zinc sulfate
Arm Title
Lactose
Arm Type
Placebo Comparator
Arm Description
270 mg lactose
Intervention Type
Drug
Intervention Name(s)
zinc sulfate
Intervention Description
zinc sulfate 220 mg bis for 90 days
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo bid for 90 days
Primary Outcome Measure Information:
Title
Severity of Facial Rosacea After 90 Days of Treatment
Description
Modified Rosacea Severity Scoring System evaluating four signs of rosacea, flushing (transient erythema or redness), erythema (redness), papules and pustules and telangiectasia (spider-veins) ranges from 0 (best, absent) to 12 (worst, severe on all items)
Time Frame
90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Diagnosis of facial rosacea made or confirmed by one of the investigators. Severity of signs of rosacea "greater than mild" at the time of enrollment. Exclusion Criteria: Treatment for rosacea during the 3 months prior to enrollment. Use of zinc dietary supplement > 25 mg per day during the 3 months prior to enrollment ( Most patients taking multivitamins with Zinc, often 15 mg per day, will not be excluded, whereas most patients taking additional Zinc supplements, often 25-50 mg per day or more will be excluded.) Diagnosis of rosacea fulminancy. Pregnant or breast feeding.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joel Bamford, MD
Organizational Affiliation
Essentia Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Mary's Duluth Clinic Health System
City
Duluth
State/Province
Minnesota
ZIP/Postal Code
55805
Country
United States

12. IPD Sharing Statement

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Zinc Sulfate in the Treatment of Rosacea: A Randomized, Controlled Trial

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