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Completed

NCT Number: NCT04058054

Skin Prick Test of KeraStat® Cream

To evaluate the potential for a humoral reaction to KeraStat Cream compared to a predicate device using the skin prick test.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

PMG Research, Inc.

Winston-Salem, North Carolina, 27103, United States

About this study

Study Overview:

Study Periods:

The length of study participation for a subject is about 2-3 days depending on availability for the final site check. There are two skin prick site checks during the course of Day 1 with a final follow up between Days 2 and 3.

Study Evaluations:

Initial screening (Screening Visit; Visit 1) will be performed on the day of the Skin Prick Test (SPT) administration and will include obtaining demographic information, brief medical history, and abbreviated physical exam.

On Day 1 (Visit 1) the SPT will be performed on the infrascapular region of the back to the right of the midline. Test articles will include the subject device (KeraStat Cream), predicate devices (KeraStat Gel, Biafine), positive control (histamine), and negative control (saline). Each test article will have a single administration, only the re-test will utilize a triplicate administration. The SPT will be ready for initial reading after approximately 15 minutes (but no sooner than 10 minutes and no longer than 20 minutes) following the final SPT administration in the series. When reading the test, the investigator will note the presence or absence of a wheal at all five sites and will measure the diameter of each wheal present. In order for the SPT to be valid, the wheal at the positive control site must exceed that at the negative control by 4 mm. If the above criteria are not met, the SPT will be repeated in triplicate on the infrascapular region of the back to the left of the midline, following the same protocol. Following the initial reading, the subject will remain at the testing facility.

A second reading will be conducted approximately 6 hours (+/- 15 minutes) after SPT administration on Day 1 (Visit 1). When reading the test, the investigator will note the presence or absence of a wheal at all five sites and will measure the diameter of each wheal present. Subjects are free to leave the clinical site after the second reading. Subjects will be instructed to promptly contact the PI and go to the ER if symptoms of an allergic reaction or shock occur.

Subjects will return to the office one to two days after initial administration for a third test reading (Visit 2). When reading the test, the investigator will note the presence or absence of a wheal in all five sites and will measure the diameter of each wheal present. Each site of test article administration will be measured for a positive reaction. A positive reaction is present when there is a measurable wheal of 3 mm or more, surrounded by a flare. Small wheals are to be confirmed by palpation. A flare alone is disregarded.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women, age 18-65
  • Able to understand the informed consent and provide written informed consent
  • Healthy, unmarked skin at the test area
  • Agreement to avoid consumption of antihistamines until completion of third test reading (Visit 2)

Exclusion criteria

  • Women who are pregnant, lactating/nursing or plan to become pregnant
  • Presence of skin disease, such as widespread urticaria or eczema
  • Diagnosis of infectious disease
  • Receiving corticosteroids, immunosuppressive agents, radiation or chemotherapy, topical growth factors, anxiolytics, imipramine, phenothiazine, dopamine, phenergen, clonidine, montelukast, immunotherapy, UV light therapy, H-2 antagonist, cyclosporine or any other medication the investigator feels will affect the test within the last month
  • Medical history of hypotension, severe hypertension, vasomotor instability, asthma, autoimmune disease, severe cardiac, pulmonary or renal disease
  • Tattoo in the intrascapular test area
  • History of surgical procedure/skin graft in the intrascapular test area
  • Employee or relative of employee of KeraNetics
  • Consumption of an anti-histamine within 7 days of the screening visit
  • History of hypersensitivity to histamine products
  • Any condition the investigator determines will compromise subject safety or prevent the subject from completing the study
  • Participated in an investigational study within 30 days of the screening visit

Treatment and study plan

KeraStat® Cream

Device

Administered 0.025 gm of KeraStat Cream per subject on day 1 of the study.

KeraStat Gel

Device

Administered 0.025 gm of KeraStat Gel per subject on day 1 of the study.

Biafine

Device

Administered 0.025 gm of Biafine per subject on day 1 of the study.

Histamine

Drug

Administered 1 drop of Histamine Dihydrocl (6 mg/mL) per subject on day 1 of the study.

Saline (0.9% NaCl)

Drug

Administered 1 drop of saline per subject on day 1 of the study.

Other names: Sodium Chloride syringe

Primary outcomes

  1. Reaction to Test Article

    Time frame: assessed at 15 min, 6 hours, 24-48 hours; 15 min reported

    Wheal measurement in millimeters (mm)

Sponsors and collaborators

Lead sponsor

KeraNetics, LLC

Industry

Registry information

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Aug 15, 2019
Registry last updated
Nov 15, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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