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Safety and efficacy of assessment of Alis collagen drink (containing 4 g hydrolyzed collagen) compared to a control collagen-free drink

Safety and efficacy of assessment of Alis collagen drink (containing 4 g hydrolyzed collagen) compared to a control collagen-free drink for improvement of biophysical and ultrasonography skin parameters

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150101020514N22
Enrollment
30
Registered
2023-09-20
Start date
2023-10-22
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

skin aging.

Interventions

Intervention 1: Intervention group: daily consumption of 250 ml of Alis collagen supplement drink for 8 weeks, which includes: Spring water, hydrolyzed bovine collagen protein (food grade) 4g, acerol

Sponsors

Pishgamane Eixire Sabze Arvand Co.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 55 Years

Inclusion criteria

Inclusion criteria: Ages 35 to 55 Healthy people with skin type II to V Signing the consent form for participation in the study

Exclusion criteria

Exclusion criteria: History of using RF, anti aging and intense pulsed light during the past 6 months .Active smoker in last 2 years Pregnancy or lactating Suffering from systemic diseases that affect skin health, such as vascular collagen diseases, diabetes, hypothyroidism, as well as liver and kidney failure. History of taking supplements containing collagen, hyaluronic acid and vitamin C in the last 3 months

Design outcomes

Primary

MeasureTime frame
Skin elasticity. Timepoint: Before intervention , 4, 8 and 12 weeks after using. Method of measurement: Cutometery.

Secondary

MeasureTime frame
Skin thickness and density. Timepoint: Before intervention ,4 , 8 and 12 weeks after using. Method of measurement: Skin ultrasound.;Changes in stratum corneum hydration. Timepoint: Before intervention , 4, 8 and 12 weeks after using. Method of measurement: Corneometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAniseh Samadi

Tehran University of Medical Sciences

dermalab@tums.ac.ir+98 21 8897 2220

Outcome results

None listed

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