A Clinical Study to Evaluate the Safety and Efficacy of a Baby Cleanser and a Moisturizer

NCT03719742 | Completed

• 1 other identifier: C18-D097
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

A Clinical Study to Evaluate the Safety and Efficacy of a Baby Cleanser and a Moisturizer Under the Supervision of Dermatologist and Pediatrician

Conditions

Atopic Dermatitis

Outcome Measures

Primary Outcomes (1)

• Eczema Area Severity Index (EASI)

  The primary efficacy endpoint is no worsening of the clinical appearance of atopic dermatitis/eczema as measured by the Eczema Area Severity Index (EASI) at week 4 from baseline. ranges from 0 (no eczema) to 72.

  4 Weeks

Secondary Outcomes (1)

• The secondary endpoint is that the sponsors test materials will be well tolerated and well perceived by subject parents/guardians according to the Family Dermatology Quality of Life Index (FDQLI)

  4 Weeks

Other Outcomes (2)

• No increase in transepidermal water loss values measured at Week 4 from baseline

  4 Weeks

• No decrease in corneometry values at Week 4 from baseline

  4 Weeks

Study Arms (1)

Sponsor Test Products

EXPERIMENTAL

1. Baby Bee Foaming Cleanser(at least once daily) 2. BB Baby Ultra Gentle Lotion (twice daily)

Other: Sponsor Test Products

Interventions

Sponsor Test Products OTHER

Baby Bee Foaming Cleanser(at least once daily but not more than twice daily), BB Baby Ultra Gentle Lotion (Once immediately after cleansing and again approximately 10-12 hours after cleansing)

Sponsor Test Products

Eligibility Criteria

• Age: 6 Months - 7 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17)

You may qualify if:

• Healthy, female or male infants/children, aged 6 months through 7 years.
• In generally good health (physical, mental, and social well-being, not merely the absence of disease/infirmity), according to parent/legal guardian report.
• Having Fitzpatrick skin type I-VI (refer to Appendix I: Fitzpatrick Skin Type).
• Having mild to moderate eczema involving 3% to 20% of body surface area, and with EASI score in the range of 1.1 to 20.0, further stratified into the following subgroups:
• Approximately 60% of subjects with clinically determined EASI score of 1.1-7.0 (mild)
• Approximately 40% of subjects with clinically determined EASI score of 7.1 to 20.0 (moderate)
• Having a parent/legal guardian at least 18 years of age who regularly bathes the child and otherwise cares for the child, and who presents proof of guardianship (eg, insurance card, certificate of residence, or copy of officially issued family registration) at the baseline visit.
• Having a parent/legal guardian willing to provide written informed consent and who can read, speak, write, and understand English.
• Whose parent/legal guardian is willing to sign a photography release.
• Willing, and having a parent/legal guardian who is willing, to cooperate and participate by following study requirements (including those outlined in section 7.3) for the duration of the study and to report any changes in health status or medications, AE symptoms, or reactions immediately.
• Willing to bring in currently used moisturizer and cleanser to visit 1 for documentation by clinic staff.

You may not qualify if:

• Diagnosed with known allergies to skin care products or ingredient(s) in the test product.
• History of skin cancer within the past 5 years.
• Individuals who have clinically active bacterial, fungal, or viral skin infections or those who have a history of recurrent cutaneous infections, according to subject self-report.
• Individuals whose use of topical corticosteroids or systemic medications for their eczema has not been stable for at least 6 weeks prior to study start. This includes medicines such as hydrocortisone, clobetasol, betamethasone, halobetasol, fluocinide, diflorasone, mometasone, halcinonide, desoximetasone, pimecrolimus, tacrolimus, crisabarole, and fluticasone.
• Having a health condition and/or pre-existing or dormant dermatologic disease on the body (eg, psoriasis, rosacea, acne \[severe acne, acne conglobata, nodules, or cysts\], seborrheic dermatitis, severe excoriations.) that the Investigator or designee deems inappropriate for participation or could interfere with the outcome of the study.
• Who have observable suntan, scars, nevi, excessive hair, tattoos, or other dermal conditions on the body that might influence the test results in the opinion of the Investigator or designee.
• Having a history of immunosuppression/immune deficiency disorders (including HIV infection, AIDS, multiple sclerosis, Crohn's disease, rheumatoid arthritis), had an organ transplant (heart, kidney, etc), or currently using oral or systemic immunosuppressive medications and biologics that are not used for the treatment of eczema (eg, azathioprine, belimumab, Cimzia, Cosentyx, cyclophosphamide, cyclosporine, Enbrel, Humira, Imuran, Kineret, mycophenolate mofetil, methotrexate, Orencia, Remicade, Rituxan, Siliq, Simponi, Stelara, Taltz) and/or undergoing radiation or chemotherapy as determined by study documentation.
• Having a disease such as asthma, diabetes, epilepsy, hypertension, hyperthyroidism, or hypothyroidism that is not controlled by diet or medication; experiencing asthma flares or having multiple health conditions.
• Having started a long-term medication within the last 2 months.
• With any planned surgeries and/or invasive medical procedures during the course of the study. Non-invasive planned surgeries will be reviewed for their impact on the study outcome and acceptability by the Investigator or designee.
• Who are currently participating in any other clinical trial at Stephens, another research facility, or doctor's office
• Infants/children with a history of or exhibiting signs and symptoms of any systemic disease that may interfere with study evaluations (eg, urinary tract infections, significant bowel or urinary congenital malformation).
• Infant/child who has had a recent change in her/his dietary intake or who has had severe diaper rash within 1 week prior to baseline.

Sponsors & Collaborators

• Burt's Bees Inc.: lead
• Stephens & Associates, Inc.: collaborator

Study Sites (1)

Stephens & Associates, Inc

Richardson, Texas, 75231, United States

Location

MeSH Terms

Conditions

Dermatitis, Atopic

Condition Hierarchy (Ancestors)

Skin Diseases, Genetic; Genetic Diseases, Inborn; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Dermatitis; Skin Diseases; Skin and Connective Tissue Diseases; Skin Diseases, Eczematous; Hypersensitivity, Immediate; Hypersensitivity; Immune System Diseases

Study Officials

• Lily Jiang, PhD

  Stephens & Associates, Inc.

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 23, 2018
• First Posted: October 25, 2018
• Study Start: September 27, 2018
• Primary Completion: January 18, 2019
• Study Completion: January 18, 2019
• Last Updated: April 19, 2019

Record last verified: 2019-04

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)