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A Study to Evaluate the Benefits of a Skincare Product on Skin Health and Appearance.

A Clinical Study to Evaluate the Efficacy of a Test Product on Hydration, Barrier Function, Sebum Regulation, Brightening, and Anti-Aging in Healthy male and female trial participants. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/07/113351
Enrollment
38
Registered
2026-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

None listed

Interventions

Intervention1: Shveta Labs Face Serum with Ghee and Rose: Apply 2 3 drops of the serum uniformly to the face and neck once daily after cleansing, and gently massage until absorbed. Control Interventio

Sponsors

Shveta Labs
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male and Female trial participants aged between 35 to 55 years both ages inclusive. 2. Participants presenting with fine lines with a score of greater or equal to 4 and wrinkles with a score of greater or equal to2, as assessed by the investigator using a validated grading scale. 3. Trial participants with facial oiliness scores between 4 and 6, as determined by the investigator. 4. Trial participants presenting with visible dark spots, acne marks, or facial hyperpigmentation. 5. Trial participants free of excessive hair, cuts, abrasions, fissures, wounds, lacerations, tattoos or any other skin conditions on their face. 6. Trial participants willing to give a voluntary written informed consent and agree to come for regular follow-up. 7. Trial participants willing to abide by and comply with the study protocol.

Exclusion criteria

Exclusion criteria: 1. Female trial participants who are pregnant or nursing or have plans of becoming pregnant during the study self-declared. 2. Trial participants taking part in another study liable to interfere with this study. 3. Trial participants with known history or present condition of an allergic response to any cosmetic product. 4. Trial participants with any other signs of significant skin irritation or skin disease or currently taking any medication, which the Investigator believes may influence the interpretation of the data. 5. Any underlying uncontrolled medical illness including diabetes mellitus, hypertension, liver disease or history of alcoholism, HIV, hepatitis, or any other serious medical illness.

Design outcomes

Primary

MeasureTime frame
1.Change from baseline to Weeks 2, 4, and 8 in dermatologist-assessed overall skin condition, including skin hydration, sebum levels, skin brightness, fine lines, wrinkles, and pigmentation scores. 2.Change from baseline to Weeks 2, 4, and 8 in skin brightness and pigmentation parameters measured by spectrophotometer. 3.Change from baseline to Weeks 2, 4, and 8 in Antera 3D-derived parameters for fine lines, wrinkles, and pigmentation. 4.Change from baseline to Weeks 2, 4, and 8 in skin hydration values measured by Corneometer. 5.Change from baseline to Weeks 2, 4, and 8 in TEWL values measured by Tewameter. Change from baseline to Weeks 2, 4, and 8 in sebum levels measured by Sebumeter.Timepoint: D1, D15, D29, D57

Secondary

MeasureTime frame
1.Change from baseline to Weeks 2, 4, and 8 in overall skin appearance parameters, including skin texture, spots, and wrinkles, as assessed by VISIA imaging analysis. 2.Change in subject self-assessment scores for hydration, smoothness, brightness, oil control, and overall skin improvement over the study period. 3.Incidence, severity, and relationship of adverse events throughout the study; dermatological tolerability assessment scores at each visit Timepoint: D1, D15, D29, D57

Countries

India

Contacts

Public ContactSudhanthiran S

MS Clinical Research Pvt. Ltd

ritambhara@msclinical.com08040917253

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026