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Nail growth among elderly women under oral collagen: a placebo-comparative study.

Evaluation of nail physiology in elderly women supplemented with hydrolyzed oral collagen: a randomized, double-blind, placebo-controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-739987q
Enrollment
Unknown
Registered
2021-11-10
Start date
2022-05-12
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Collagen. Nails. Elderly

Interventions

Experimental group: 40 elderly women will receive supplementation of 2.5g / day hydrolyzed oral collagen for 12 weeks. Control group: 40 elderly women will receive collagen-like sachets containing pla
SP6.051.227

Sponsors

Faculdade de Medicina de Botucatu (FMB Unesp)
Lead Sponsor
Faculdade de Medicina de Botucatu (FMB Unesp)
Collaborator

Eligibility

Sex/Gender
Female
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: Women with more than 60 years; residents of the Botucatu-SP region; who agreed to participate in the study

Exclusion criteria

Exclusion criteria: Immunocompromised women or those using immunosuppressive drugs; diabetics; using anticoagulants or coagulation disorders; using oral retinoids; vegetarians; in protein supplementation; with kidney diseases; thyropathies and nail diseases and current clinical diagnosis will not be included previous or evidence of any medical condition that exposes the patient to increased risks or interferes with the safety or efficacy of the proposed treatment.

Design outcomes

Primary

MeasureTime frame
To evaluate the nail growth rate through digital photography; it is expected to find a 10% higher increase in nail growth speed in the group that received oral collagen compared to the placebo group;To evaluate the thickness of the dermis through ultrasound; it is expected to find a 10% greater increase in the thickness of the dermis in the group that received oral collagen compared to the placebo group;To evaluate the thickness of the nail plate through ultrasound; it is expected to find a 10% greater increase in nail plate thickness in the group that received oral collagen compared to the placebo group ;To assess the strength of the nail plate through a durometer; it is expected to find 10% greater increase in nail plate strength in the group that received oral collagen compared to the placebo group

Secondary

MeasureTime frame
Assess the improvement of photoaging through the forearms photoaging scale; it is expected to find a reduction in the forearms photoaging scale greater than 10% in the group that received oral collagen in relation to the placebo group;Evaluate the increase in the average thickness of the hair strands through trichoscopy; it is expected to find a 10% greater increase in hair thickness in the group that received oral collagen compared to the placebo group

Countries

Brazil

Contacts

Public ContactMariana;Tatiana De Ré;Polo

Faculdade de Medicina de Botucatu (FMB Unesp);Faculdade de Medicina de Botucatu (FMB Unesp)

mariana.righetto@unesp.br;tatiana.figueira@yahoo.com.br+55-41-99188907;+55-14-99186-0089

Outcome results

None listed

Source: REBEC (via WHO ICTRP)