Burn Scar, Itch Scarring, Wound
Conditions
Keywords
Itch, Burn, Diphenhydramine, Famotidine
Brief summary
The purpose of the study is to see whether using diphenhydramine (Benadryl), famotidine (Pepcid), and cromolyn sodium will decrease burn scar itch.
Detailed description
The purpose of this study is to examine the effect of a new approach to treating burn scar itch. In other patient populations experiencing itch, H2 antihistamines and/or topically applied cromolyn sodium have decreased itch. We believe that these medications will reduce itch from burn scars. To test this idea, the investigators will compare two methods of treating itch: 1) recommended oral diphenhydramine (Benadryl) with placebo capsule and placebo lotion and 2) recommended oral diphenhydramine (Benadryl) with administration of oral famotidine (Pepcid) and topically applied cromolyn sodium.
Interventions
COMBINATION_PRODUCTFamotidine and 4% topical cromolyn sodium
Patients will be instructed to take a 20mg famotidine capsule twice daily, and to use the lotion (4% cromolyn sodium) twice daily.
OTHERPlacebo
Treatment with active H1 antihistamine plus administration of placebo famotidine and placebo cromolyn sodium.
Sponsors
University of Texas
The University of Texas Medical Branch, Galveston
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
Participants must meet all the inclusion criteria in order to be eligible to participate in the study. * Participant has provided informed consent in a manner approved by the IRB and is willing and able to comply with the trial procedures. * Adults: ≥18 to \<80 years of age. * Has an itchy burn scar.
Exclusion criteria
Participants meeting any of the
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Itch Scale: Visual Analogue Scale Itch (VAS Itch) | baseline, weekly for 3 months, at 3 and 6 months (+/-15 days each timepoint) after start date | Patients will score the severity of itch on the scale provided at study start, once weekly for 3 months, at the 3-month visit, and again at study end (6 months). Patients will rate their itch from 0 to 10. to measure the intensity of itchiness, where a patient marks a point on a line to indicate how severe their itch is, with zero representing no itch and 10 representing worst imaginable itch. A higher score means a worse outcome. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Brisbane Burn Scar Impact Panel (BBSIP) | baseline, and at clinic visit approximately 3 months (±15 days) after study start | BBSIP is a patient-reported outcome measure developed in consultation with burn survivors that takes approximately 10 minutes to complete; the specificity of this comprehensive questionnaire allows detection of changes in quality of life related to burn hypertrophic scar. Higher scores indicate a worse outcome. |
| PROMIS-29 | baseline, and at clinic visit approximately 3 months after study start (±15 days) | This questionnaire will be administered to determine whether the effects of treatment impact quality of life as reported by the patient. |
| The Patient and Observer Scar Assessment Scale 3.0 | baseline, and at clinic visit approximately 3 months (±15 days) after study start | The Patient and Observer Scar Assessment Scale (POSAS) is an established scale for assessing scars by both the patient and the observer. The overall opinion of the scar is reported on a scale of 1-10, with 1 being normal skin and 10 being the worst scar. (POSAS 3.0) will be filled out by the participant and a clinical observer to evaluate scar severity/quality. |
| Patient Global Impression of Change (PGIC) | baseline, and at clinic visit approximately 3 months after study start (±15 days) | A global index that consists of 3 questions to which participants will rate the severity of 1) their PAH symptoms, 2) shortness of breath (SOB), and 3) fatigue. The minimum and maximum range of scores for each of the 3 individual questions was 1-5, with severity scale choices of 1=not present, 2=mild, 3=moderate, 4=severe, and 5=very severe. A higher score indicates a worse outcome. |
| Participants Activity with Fitbit | Month 1, 2, 3 (+15 days, each timepoint) | Overall activity: To be captured via Fitbit on a daily basis to gauge overall activity. These data will be correlated with the itch and pain scales, as reduced activity is associated with pain and/or itch. |
| Pain scale: Visual Analog Scale for Pain (VAS Pain) | baseline, and at clinic visit approximately 3 months and 6 months after study start (±15 days) | The VAS pain score is a simple and effective method used to measure patients' pain levels. This method is typically represented by a line ranging from 0 to 10, where 0 indicates no pain and 10 indicates the most severe pain. Patients are asked to mark a point on the line that corresponds to their level of pain. |
Countries
United States
Contacts
Primary ContactLindsey Allen, RN
Outcome results
None listed