Seborrheic Dermatitis Clinical Trial
Official title:
Safety and Efficacy of SEBORRHEAMEDIS Face Cream in Patients With Seborrheic Dermatitis
Verified date | March 2015 |
Source | Kamedis Ltd. |
Contact | n/a |
Is FDA regulated | No |
Health authority | Spain: CEIC Puerta hierro |
Study type | Interventional |
SEBORRHEAMEDIS Face Cream is a barrier-based, non-steroidal cream. The cream includes plant extracts The cream was designed to manage the symptoms of facial Seborrheic dermatitis symptoms such as erythema, scaling and pruritus.
Status | Completed |
Enrollment | 30 |
Est. completion date | December 2015 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Subject with mild (ISGA=2) to moderate (ISGA=3) facial Seborrheic dermatitis. - Male or female aged 18 years or older. - Subject who agrees not to use any Seborrheic Dermatitis medication during the study, except for the tested product. - Subject is willing to sign an Informed Consent Exclusion Criteria: - Subject pregnant or lactating. - Subject has a condition that requires continuous systemic or topical corticosteroid or antimycotic therapy - Subject has a severe disease that is likely to interfere with the study conducting - Subject has a known sensitivity to any of the ingredients contained in the tested product. - Subject is expected to be extensively exposed to the sun during the study |
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Kamedis Ltd. |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Improvement of overall ISGA. Descriptive Name of scale. Physician dermatology evaluation. | Days 42 | Yes | |
Secondary | Improvement of erythema, desquamation on the target area. Physiological parameter. Physician dermatology evaluation. | Days 0, 14, 28 and 42 | Yes | |
Secondary | Improvement of pruritus. Physiological parameter. Assessed by subject. | Days 0, 14, 28 and 42 | Yes | |
Secondary | Number and severity of Adverse Events | Days 0, 14, 28 and 42 | Yes |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01703793 -
Safety and Efficacy Study in Subjects With Seborrheic Dermatitis
|
Phase 2 | |
Completed |
NCT01203189 -
Seborrheic Dermatitis: Ketoconazole 2% Foam Versus Ketoconazole 2% Shampoo
|
N/A | |
Completed |
NCT00991198 -
The Role of Topically Dissolved Oxygen (TDO) to Ameliorate Signs of Photodamage
|
Phase 2 | |
Completed |
NCT03567980 -
A Proof of Concept Clinical Trial Evaluating the Safety and Efficacy of Eucrisa (Crisaborole) in Patients With Seborrheic Dermatitis
|
Phase 4 | |
Recruiting |
NCT03688971 -
Omiganan Twice a Day (BID) in Patients With Facial Seborrheic Dermatitis
|
Phase 2 | |
Recruiting |
NCT01139749 -
Efficacy and Safety of Low-dose Oral Isotretinoin for Seborrhea
|
Phase 4 | |
Completed |
NCT05105139 -
Study to Evaluate the Safety of Sebryl® and Sebryl Plus® in Seborrheic Dermatitis and Psoriasis of Scalp
|
||
Completed |
NCT01591070 -
Proactive Treatment of Tacrolimus Ointment for Adult Facial Seborrheic Dermatitis
|
Phase 4 | |
Completed |
NCT05787860 -
Ruxolitinib in Seborrheic Dermatitis
|
Phase 2 | |
Completed |
NCT00403559 -
A 4 Week Study of Elidel (Pimecrolimus) for the Treatment of Seborrheic Dermatitis
|
Phase 2 | |
Not yet recruiting |
NCT00767546 -
Botulinum Toxin for Treatment of Seborrhic Dermatitis in Parkinsonian Patients
|
Phase 1 | |
Terminated |
NCT01315951 -
Petrolatum's Effect on Initial Symptoms of Nonscalp Seborrheic Dermatitis and Preventing Exacerbation
|
N/A | |
Recruiting |
NCT05942248 -
The Use of Image-Based Computer Gradings in the Analysis of Acne, Rosacea, Melasma, and Seborrheic Dermatitis
|
N/A | |
Recruiting |
NCT06013371 -
PDE4 Inhibition in Seborrheic Dermatitis and Papulopustular Rosacea
|
Phase 2 | |
Recruiting |
NCT05319444 -
Cleansing Device for the Treatment of Scalp and Hair Conditions
|
N/A | |
Completed |
NCT04445987 -
Long-Term Safety of ARQ-154 Foam in Subjects With Seborrheic Dermatitis
|
Phase 2 | |
Completed |
NCT04973228 -
Trial of PDE4 Inhibition With Roflumilast (ARQ-154) Foam 0.3% for the Management of Seborrheic Dermatitis (STRATUM)
|
Phase 3 | |
Completed |
NCT03114111 -
Pilot Study for the Use of Photodynamic Therapy in the Treatment of Seborrheic Dermatitis
|
Early Phase 1 | |
Completed |
NCT00830908 -
HairMax LaserComb Open Label Study to Treat Seborrheic Dermatitis
|
N/A | |
Completed |
NCT02349854 -
Neurobiology of the Scalp in Seborrheic Dermatitis
|
N/A |