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Assessment of Steroneo Skin Cream (Physalis Angulata Supercritical Extract) application for treatment of eczematous lesions

Assessment of Efficacy, Tolerability and Safety of Steroneo Skin Cream (Physalis Angulata Supercritical Extract) application for treatment of eczematous lesions: A Prospective, Open-label, Non-Comparative Study

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2016/11/007511
Enrollment
50
Registered
2016-11-30
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Eczema of skin

Interventions

Intervention1: Steroneo Skin Cream: 30gm of Physalis Angulata Supercritical Extract used topically twice a day

Sponsors

Rehmat Clinic
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Clinically diagnosed with eczematous lesions of any of the following types and requiring mild to moderate topical steroid therapy: • Atopic dermatitis • Contact dermatitis • Xerotic eczema • Nodular eczema • Seborrheic dermatitis • Neurocutaneous dermatitis (lichen simplex chronicus) • Drug eruptions, photo-dermatitis • Pruritus requiring topical corticosteroids Patients/parents who sign the written informed consent form Patients willing to and able to understand and comply with all study requirements

Exclusion criteria

Exclusion criteria: 1. Patients having any of the following conditions: • Lichen planus • Severe dermatitis requiring systemic corticosteroids • Infantile dermatitis 2. Patients requiring systemic corticosteroids on any form 3. Pregnant and lactating women 4. Patients with known hypersensitivity to any of the ingredients/excipients of the study cream 5. Any other condition, which in the opinion of the clinician/investigator, could interfere significantly with the treatment and assessment process 6. Use of any investigational therapy within 30 days prior to randomization 7. Patients not willing to provide written informed consent

Design outcomes

Primary

MeasureTime frame
To assess the efficacy of Steroneo Physalis Angulata Supercritical Extract application for treatment of eczematous lesions.Timepoint: 12 weeks.

Secondary

MeasureTime frame
Dermatology Life Quality Index would be assessed using a 10 item questionnaire by patients above 16 years of age Reduction in number and size of lesions of eczema. Appearance of new lesions of eczema. Pruritus Score will be assessed on a scale of 0 to 3. Erythema will be assessed on a scale of 0 to 3. Global assessment of response to therapy evaluated by the doctors on a 5point scale. Global assessment of tolerability to therapy would be assessed by the patients on a 5point scale. Timepoint: 12 weeks

Countries

India

Contacts

Public ContactRashid Shaikh

Rehmat Clinic

dr.rashidshaikh@gmail.com9820366255

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026