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To Evaluate the Effects of Nutrova Collagen+Antioxidants on Hair Health Parameters

An Open-Label Case Series to Evaluate the Safety and Efficacy of Nutrova Collagen+Antioxidants on Hair Health Parameters - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/03/107013
Enrollment
40
Registered
2026-03-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

None listed

Interventions

Intervention1: Nutrova Collagen+Antioxidants: 1 sachet to be taken once daily, orally, mixed with plain water, after a meal for 90 days Control Intervention1: NA: NA

Sponsors

AXYS NUTRITION PRODUCTS PRIVATE LIMITED
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: To be eligible for the study, Subjects must meet the following criteria: Healthy women aged 25 to 48 years Experiencing excessive hair fall and/or visible hair thinning Willing to consume a marine collagen (fish-derived) supplement Willing to take the supplement daily for 90 days No hair transplant, PRP, laser therapy, or other scalp procedures in the past 6 months Not currently using hair growth medications (oral or topical) and willing to avoid starting new treatments during the study No scalp dermatologic condition that interferes with assessment Willing to provide written informed consent

Exclusion criteria

Exclusion criteria: Subjects with any of the following conditions will be excluded from the study: Known allergy to fish, marine collagen or any component of the supplement Pregnancy or breastfeeding Have systemic illness affecting hair growth (e.g., uncontrolled thyroid disorder, autoimmune disease) or active scalp infections or inflammatory scalp disorders Participation in another clinical study in the last 30 days Have used minoxidil, finasteride, PRP, or similar treatments within 3 months

Design outcomes

Primary

MeasureTime frame
1. Objective Hair Density & Thickness (Objective Instrument-Based Assessment) Measured using Tricoscope at: Frontal scalp Temporo-parietal region Parameters: Hair density (hair/cm ) Hair shaft thickness ( m) Primary outcome: Change from Baseline (Day 0) to Day 90 This endpoint directly quantifies the effect of Nutrova Collagen+Antioxidants on scalp dermal collagen remodeling and surface smoothness. This will help determine the effect of the intervention on the treatment outcome. Timepoint: Baseline (Day 0) Day 45 Day 90

Secondary

MeasureTime frame
Participant-Reported Outcomes Assessing perceived hair improvement using a questionnaire: Hair thickness Hair volume Hair breakage & hair fall Hair texture Hair growth On Day 45 & Day 90, the participant has to rate the following on a scale from 1 to 5 (1 = Strongly Disagree, 5 = Strongly Agree): 1. I feel that my overall hair fall has reduced compared to before starting the product. 2. I experience less hair breakage during washing, combing, or daily grooming. 3. I feel that new hair growth has improved since starting the product. 4. I notice improved coverage or reduced visibility of scalp in thinning areas. 5. My hair feels thicker than it did before starting the product. 6. My hair looks fuller & more voluminous. 7. My hair texture feels smoother. 8. My hair feels/looks healthier overall. Timepoint: Day 45, Day 90

Countries

India

Contacts

Public ContactDr Meghna Motwani

Axys Nutrition Products Private Limited

meghna.motwani@nutrova.com9867144003

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026