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Study to Evaluate the Efficacy of Blue Fenugreek Kale Extract (BFKE) on Skin

A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy of Blue Fenugreek Kale Extract (BFKE) on Skin.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04544982
Enrollment
60
Registered
2020-09-10
Start date
2020-09-01
Completion date
2021-03-25
Last updated
2021-04-06

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

Conditions

Skin Health

Brief summary

Participants will be supplemented BFKE for a period of 8-weeks to improve skin health. The objective of the study is to evaluate the 'Transepidermal Water Loss (TEWL)' that characterizes the skin barrier function of stratum corneum. Additional parameters include, evaluation of skin moisture content, wrinkling, elasticity, sagging, radiance and also on inflammatory biomarkers.

Interventions

OTHERBlue fenugreek kale extract

One capsule to be taken orally before breakfast and one capsule after lunch, with water.

OTHERPlacebo

One capsule to be taken orally before breakfast and one capsule after lunch, with water.

Sponsors

Vedic Lifesciences Pvt. Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
30 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy, adult female participants aged ≥ 30 and ≤ 55 years. * Participants with signs of poor skin barrier as determined by Trans-epidermal water loss ≥ 15 g/m2/h on forehead. * Participants with skin type II to IV as per Fitzpatrick skin type calculator. * Participants with skin type II and III as per Glogau's classification of photoageing skin. * Participants must have Body Mass Index (BMI) ≥ 18.5 ≤ 29.9 kg/m2. * Participants with moderate signs of Melasma as assessed by the investigators. * Participants ready to abstain from any cosmetic or drug-based cream, ointment, lotion and other products apart from the ones allowed during study period. * Participants ready to rinse their face only with water and to refrain from using soap, facewash, make-up etc. or any other cosmetic care related products 12 hrs. prior to any assessment visit.

Exclusion criteria

* Unwilling to forgo any aesthetic or dermatological treatments or procedures during the study period. * Participants with visible scarring on face. * Participants having any form of skin disorder on the Nasolabial fold. * Water consumption history of ≤ 500 ml and ≥ 3000 ml per day. * Smoking or using any tobacco products. * Participants presently undergoing or had undergone treatment for softening or reducing wrinkles in the last 3 months. * Having a history of chronic skin allergies. * History of heavy caffeine usage ≥ 4 cups in a day. * Binge drinkers as defined by consumption of 4 or more alcohol containing beverages within 2 hours. * Presence of unstable, acutely symptomatic, or life-limiting illness. * Participants taking any vitamins and other related supplements. * Menopausal and peri-menopausal females. * Females who are pregnant/planning to be pregnant/lactating or taking any oral contraceptives. * Females who have had participated in a study of an investigational product 90 days prior to the screening.

Design outcomes

Primary

MeasureTime frameDescription
Investigator's global assessment using 5-point Likert scaleFrom Base line Day 0 to day 56The Study Investigator will assess on a scale of 0 (Very poor) to 4 (Excellent) as to how beneficial or vice-versa was the treatment experience over the study period.
Trans Epidermal Water Loss (TEWL) using Tewameter®.From Base line Day 0 to day 56To evaluate the effect of 8-week consumption of BFKE on skin barrier function as evaluated by Trans Epidermal Water Loss (TEWL) using Tewameter®.
Skin moistureFrom Base line Day 0 to day 56skin hydration as measured by skin moisture (forehead & forearm) using skin moisture analyzer.
Modified Fitzpatrick Wrinkle Severity ScaleFrom Base line Day 0 to day 56Changes in the wrinkle class from Class 3.0 indicated worst means Deep wrinkle. Deep and furrow wrinkle; more than 3-mm wrinkle depth to Class 0 indicates Good means No wrinkle. No visible wrinkle; continuous skin line.
Ezure Sagging scaleFrom Base line Day 0 to day 56Cheek with Highest sagging score means Very severe sagging indicates worst and Lowest sagging score means No sagging indicates better
Pinch recoil testFrom Base line Day 0 to day 56A decrease in pinch recoil time is associated with improvement in skin elasticity/firmness.
Skin parameters using a participant based self-assessment questionnaireFrom Base line Day 0 to day 56Highest Score represents Better and lowest Score represents Worst
Participant's global assessment using 5-point Likert scaleFrom Base line Day 0 to day 56The Participant will self-assess on a scale of 0 (Very poor) to 4 (Excellent) as to how beneficial or vice-versa was the treatment experience over the study period.
Inflammatory biomarkersFrom Base line Day 0 to day 56Change in the levels of Inflammatory biomarkers within specified range
Allergic skin inflammation as assessed by Eosinophil to basophil ratio and Neutrophil to lymphocyte ratio.From Base line Day 0 to day 56Change in the levels of Eosinophil to basophil ratio and Neutrophil to lymphocyte ratio within specified range
Oxidative Stress as assessed by Malondialdehyde concentration.From Base line Day 0 to day 56malondialdehyde concentration of the samples will be measured as an index of lipid peroxidation

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026