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A Clinical Trial to Evaluate the Efficacy of Ghee Sutra Face Emulsion in Improving Facial Skin Aesthetics

A Randomized Open Labelled Clinical Trial to Evaluate the Efficacy of Ghee Sutra Face Emulsion in Improving Facial Skin Aesthetics - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056710
Enrollment
30
Registered
2023-08-21
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

None listed

Interventions

None listed

Sponsors

Sriveda Sattva Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Healthy human subjects between the age group of 18-60 years irrespective of their gender and willing to give written consent preferably with fair representation of all age group subsets 2.Subjects with Hyperpigmentation skin rashes Rosacea Dark spots Reduced smoothness softness tonicity and hydrated appearance of skin 3.Subjects whose facial skin is free of dermatological diseases like eczema wounds inflammatory scar or any systemic disease with facial dermatological implications 4.Subjects willing to come for regular follow up and ready to follow the instructions proposed during the study period 5.Subjects representing varied skin types ideally with fair representation of all 4 skin types namely Oily Normal Dry and Combination

Exclusion criteria

Exclusion criteria: 1.Subjects with diagnosed or highly probable allergy to one or more compounds or active ingredients of any cosmetic product 2.Subjects with known allergic reactions to perfumes and /or preservatives used in cosmetic products 3.Subjects with any acute or chronic skin diseases or any systemic disease with facial dermatological implications 4.Subjects who have changed their cosmetic habits /facial skin care habits within the past 14 days preceding the start of trial 5.Subjects undergoing hormonal therapy since past 12 weeks or less prior to the start of study 6.Subjects who are daily exposed to sun for long hours 7.Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
1.Changes in Investigator’s Global Assessment(IGA) scale of Hyperpigmentation and Erythema 2.Changes in Investigator’s Global Assessment(IGA) scale of Rosacea severity 3.Changes in Allergan Skin Roughness scale 4.Changes in Overall Dry Skin scoreTimepoint: 7th Day 14th Day 21st Day 28th Day

Secondary

MeasureTime frame
Changes in Subject Global Aesthetic Improvement scale with respect to skin hydration & tonicityTimepoint: 7TH DAY 14TH DAY 21ST DAY 28TH DAY

Countries

India

Contacts

Public ContactDr Shema Sara Kurien

SRI SRI COLLEGE OF AYURVEDIC SCIENCE AND RESEARCH HOSPITAL

sajithak96@gmail.com7760987722

Outcome results

None listed

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