Evaluation of an Under-Eye Cream Containing Retinol and Pycnogenol for Reducing Dark Circles in Adults Aged 18 to 60 Years Over 16 Weeks

Evaluation of an Under-Eye Cream: Open-label Single Arm Interventional Prospective Study - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/07/090872

Enrollment

Registered

2025-07-14

Start date

Unknown

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

None listed

Interventions

Intervention1: Open Label Single Arm Interventional Prospective Study: An Under eye cream will be given to all the participants Night-time Use: Make sure the skin is clean and dry before application.

Eligibility

Inclusion criteria

Inclusion criteria: 1)18 60 years 2)Visible under-eye pigmentation 3)Consent to participate 4)Comply with follow-up schedule

Exclusion criteria

Exclusion criteria: 1)Recent use of topical depigmenting agents on the face(past 4 weeks) 2)Known allergy to any ingredient in the cream Ongoing dermatological or systemic illness affecting the face 3)Pregnant or lactating women

Design outcomes

Primary

Measure	Time frame
Improvement in the pigmentary, vascular or mixed type of peri orbital hyperpigmentation Timepoint: Day 0, Week 4,8,12 & 16	—

Secondary

Measure	Time frame
To evaluate participant-reported outcomes, including self-assessed wrinkle improvement and satisfaction with the appearance of their under-eye area. Timepoint: Day 0, Week 4,8,12 & 16	—

Countries

India

Contacts

Public ContactDr.T.Vanathi

Render Skin and Hair

drvanathi@renderclinic.com9884748215

Outcome results