Prospective Placebo-controlled Study of Synochi Scar Spray

Launched by SYNOCHI, LLC · Nov 17, 2021

Keywords

ClinConnect Summary

This clinical trial is studying a product called Synochi Scar Spray to see if it can help improve the appearance of scars in people who have experienced severe burns and received skin transplants. The study will involve healthy participants aged 22 to 50 years who have both a burn scar and a skin donor site that are at least six weeks old. Participants must be in good health and able to understand the study procedures in English. They also need to agree to share photos and videos of their scars during the trial.

If you join this study, you will be randomly assigned to either receive the Synochi Scar Spray or a placebo (a spray that doesn’t contain the active ingredient) for nine months. Throughout the study, your scar will be documented with photos, and you will be asked to fill out questionnaires about your experience. After the treatment period, there will be an additional three months of follow-up to assess the results. It's important to note that participants cannot have any serious health conditions that could interfere with the study and must not be involved in other clinical trials during this time.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • - Study participants are healthy study participants from any sex and race, but must be between 22 and 50 years of age at the time of consent.
• • Study participants must be willing to provide written informed consent and be able to read, write, speak, and understand the test procedures in English. Ability will be documented with a doctors' note.
• • Study participants must be willing to sign a Photo and Video Release Form.
• • Study participants must possess both the original burn scar area that is the skin graft recipient area and the skin graft donor site that is at least around 6 weeks old that have not been altered in any way prior (No prior scar reduction surgery, laser, steroid injections, silicone sheets or anything of the like).
• • Study participants must be in good general health.
• Exclusion Criteria:
• • - Study participants must not currently be under the care of a medical or cosmetic professional for care of the scar to be evaluated in testing.
• • They must be without medical diagnosis of medicated or uncontrolled diabetes, hepatitis B, hepatitis C, an organ transplant, a heart murmur, mitral valve prolapse with heart murmur, fibromyalgia, ulcerative colitis, Crohn's disease, moderate to severe asthma (requiring daily use of systemic steroid medication, nasal steroids are permitted), an immunocompromised condition such as AIDS (or HIV positive), lupus, or medicated multiple sclerosis, not pregnant or trying to become pregnant, lactating, transplant recipient on immunosuppression, the BMI should be 19 - \< 35.
• • Have any type of vascular disease (e.g., arteriosclerosis, Raynaud's Syndrome, or peripheral venous disease) or any blood clotting disorders.
• • Have participated in another clinical study within the past 14 days, or be currently participating in another clinical study.
• • Have or have someone in their household with known sensitivities or allergies to latex (rubber), bar or liquid cleansing products, serums, moisturizers, lotions, creams, preservatives, fragrances, cosmetics, or common ingredients used in traditional Chinese medicine, including Notopterygium root (Notopterygium Incisum), sweetgum fruit ( Liquidambaris Fructus), bur reed rhizome (Rhizoma Sparganii), corydalis rhizome (Rhizoma Corydalis), ledebouriella root / siler (Radix Saposhnikoviae), costus root (Radix Auklandiae Lappae), rehmannia root (Radix Rehmanniae Preparata), deer horn gelatin/glue (Gelatinum Cornu Cervi), safflower (Carthamus Tinctorius), forsythia fruit (Fructus Forsythiae), red earthworm (Lumbricus), trichosanthes root (Radix Trichosanthes), Chinese motherwort (Herba Leonuri), millettia vine (Caulis Spatholobi), zedoary rhizome (Rhizoma Curcumae), turmeric tuber (Radix Curcumae), rhubarb (Radix et Rhizoma Rhei), white peony root (Radix Paeoniae Alba), white mustard seed (Semen Sinapis Albae), Chinese angelica root (Angelicae sinensis Radix), cinnamon twig (Ramulus Cinnamomi), red peony (Radix Paeoniae Rubra), peach kernel (Semen Persicae), astragalus (Radix Astragali), frankincense resin (Resina Boswelliae Carterii), myrrh (Resina Commiphorae Myrrhae), sandalwood (Santalum Album), radiz notoginseng (Radix Notoginseng), spine of honey locust (Spina Gleditsiae), silkworm (Bombyx Batryticatus)
• • Have experienced hives (raised welts) as a reaction to anything contacting their skin.
• • Not be diagnosed with a medical condition that, in the opinion of the Principal Investigator, would preclude participation.
• • Not be unwilling to fulfill the performance requirements of the study.
• • Not be direct employees, in a relationship with, or family of the sponsor or Principal Investigator.
• • Not be participating in any other clinical trial during the time of this clinical trial.
• • Medication: Not be receiving any steroid medications (including those used to treat asthma) other than for contraception, hormone therapy, or menopausal purposes. No chemotherapeutic agents or any medication that interferes with wound healing (rheumatologic agents, Emgality or Aimovig).