New Topical Treatment for Continued Pain After Shingles
Primary Purpose
Postherpetic Neuralgia
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Epikeia coatings with aspirin
Epikeia coatings with lidocaine
Epikeia coatings alone
Sponsored by
About this trial
This is an interventional treatment trial for Postherpetic Neuralgia focused on measuring Post-herpetic Neuralgia, Pain after Shingles, Shingles, PHN
Eligibility Criteria
Inclusion Criteria:
- In good general health
- Postherpetic neuralgia, defined as pain persisting more than 4 months after onset of herpes zoster outbreak
- Willing to use effective forms of contraception for the duration of the study
Exclusion Criteria:
- Known lidocaine sensitivity or allergy
- Inability to discontinue use of any nonstudy lidocaine-containing products for the duration of the study
- Known hypersensitivity to aspirin
- Open herpes zoster blisters
- Known sensitivity or allergy to an amide-type local anesthetic agent
- Existing conditions that make participation unsafe
- Pregnant
- Immunocompromised (e.g., HIV infected)
- Herpes zoster in any dermatome (area of skin innervated by a specific sensory nerve) affecting the face or scalp
- Affected skin area is greater than 420 square cm
- Affected area includes skin breakdown or nonintact skin
- Affected area consists of more than one contiguous area
Sites / Locations
- Dermatology Clincial Reseach Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
1
Arm Description
Participants will receive one of three different topical treatments on Days 8, 15, or 22.
Outcomes
Primary Outcome Measures
Latency to analgesia onset and duration of analgesia measures
Secondary Outcome Measures
Skin irritation potential
Full Information
NCT ID
NCT00566904
First Posted
September 10, 2007
Last Updated
August 29, 2011
Sponsor
Biomedical Development Corporation
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), The University of Texas Health Science Center, Houston
1. Study Identification
Unique Protocol Identification Number
NCT00566904
Brief Title
New Topical Treatment for Continued Pain After Shingles
Official Title
Phase 1 Novel Topical Treatment for Post-herpetic Neuralgia
Study Type
Interventional
2. Study Status
Record Verification Date
August 2011
Overall Recruitment Status
Completed
Study Start Date
September 2006 (undefined)
Primary Completion Date
August 2008 (Actual)
Study Completion Date
September 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Biomedical Development Corporation
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), The University of Texas Health Science Center, Houston
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Shingles is an outbreak of rash or blisters on the skin that is caused by the same virus that causes chicken pox. Some people experience continued pain even after the shingles rash and blisters have healed; this pain is known as postherpetic neuralgia. The purpose of this study is to evaluate the effectiveness of a new topical treatment for postherpetic neuralgia in adults.
Detailed Description
After an initial infection of chicken pox, the varicella-zoster virus can remain dormant inside nerve cells. Years later, the virus can be reactivated, causing a repeat outbreak called shingles. The first symptom of shingles is usually a burning or tingling pain in one particular location and on one side of the body. This pain can range from mild to severe. Other possible symptoms of shingles include numbness and itching. After several days or 1 week, a rash of fluid-filled blisters similar to chicken pox appears. For most healthy people, a case of shingles heals within a month. However, some people continue to feel pain after the rash and blisters have resolved; this pain is known as postherpetic neuralgia. Current treatments for postherpetic neuralgia include antiviral drugs, steroids, antidepressants, anticonvulsants, and topical products. A new topical treatment consists of a liquid product that is applied directly to the skin to let dry and form a thin, transparent barrier film. In contrast to creams or ointments that can stay in contact with skin for only minutes, this product remains intact on the skin for many hours, providing sustained delivery of a drug or medication while maintaining barrier protection for the skin. The purpose of this study is to evaluate the effectiveness of this new topical treatment for postherpetic neuralgia in adults.
This study will last about 3 weeks and will include seven study visits on Days 1, 8, 9, 15, 16, 22, and 23. All study visits will include questionnaires on pain levels and an examination and digital photos of the affected skin area. The study visit on Day 1 will also include a urine pregnancy test and a review of medical and medication history. During the study visits on Days 8, 15, and 22, one of three topical products will be applied to participants' affected skin. The product will dry on the skin in 30 to 45 seconds. Participants will then wait at the study site for 1.5 hours, after which they will record the time when they experienced pain relief. At each of these three treatment visits, participants will receive one of the following three topical products: Epikeia coatings with aspirin, Epikeia coatings with local anesthetic, and Epikeia coatings alone. At these three study visits, questionnaires, examinations, and digital photographs will occur both before and after the products are applied to the skin. Throughout the study, participants will record their pain levels and medications in a diary, which will be reviewed at all study visits.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postherpetic Neuralgia
Keywords
Post-herpetic Neuralgia, Pain after Shingles, Shingles, PHN
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Participants will receive one of three different topical treatments on Days 8, 15, or 22.
Intervention Type
Drug
Intervention Name(s)
Epikeia coatings with aspirin
Other Intervention Name(s)
Epikeia coatings with acetylsalicylic acid
Intervention Description
Applied to affected skin area using a roll-on ball applicator
Intervention Type
Drug
Intervention Name(s)
Epikeia coatings with lidocaine
Other Intervention Name(s)
Epikeia coatings with local anesthetic
Intervention Description
Applied to affected skin area using a roll-on ball applicator
Intervention Type
Other
Intervention Name(s)
Epikeia coatings alone
Intervention Description
Applied to affected skin area using a roll-on ball applicator
Primary Outcome Measure Information:
Title
Latency to analgesia onset and duration of analgesia measures
Time Frame
Between 8 and 16 hours after treatment application
Secondary Outcome Measure Information:
Title
Skin irritation potential
Time Frame
Between 8 and 24 hours after treatment application
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
In good general health
Postherpetic neuralgia, defined as pain persisting more than 4 months after onset of herpes zoster outbreak
Willing to use effective forms of contraception for the duration of the study
Exclusion Criteria:
Known lidocaine sensitivity or allergy
Inability to discontinue use of any nonstudy lidocaine-containing products for the duration of the study
Known hypersensitivity to aspirin
Open herpes zoster blisters
Known sensitivity or allergy to an amide-type local anesthetic agent
Existing conditions that make participation unsafe
Pregnant
Immunocompromised (e.g., HIV infected)
Herpes zoster in any dermatome (area of skin innervated by a specific sensory nerve) affecting the face or scalp
Affected skin area is greater than 420 square cm
Affected area includes skin breakdown or nonintact skin
Affected area consists of more than one contiguous area
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adelaide A. Hebert, MD
Organizational Affiliation
The University of Texas Health Science Center, Houston
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dermatology Clincial Reseach Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
12. IPD Sharing Statement
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New Topical Treatment for Continued Pain After Shingles
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