Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07322653

The Effects of MediDrink Platinum+ and Fava Bean Protein Hydrolysate on Fitness in an Aged Population

Prospective, Open-Label, Multicenter Study to Characterise the Effects of Co-administration of MediDrink Platinum+ Formula Containing Novel Protein Blend SPR-01 and Fava Bean Protein Hydrolysate on Fitness in an Aged Population

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
75 (estimated)
Sponsor
Nuritas Ltd · Industry
Sex
All
Age
60 Years
Healthy volunteers
Not accepted

Summary

Examining the effects of MediDrink Platinum+ containing novel protein blend SRP-01 alone or when combined with PeptiStrong on clinical responses in elderly adults with sarcopenia

Detailed description

The primary aim of this multicentre randomised active control group study , is to characterise the effect of MediDrink Platinum+ containing a novel protein blend SPR-01, alone and in combination with PeptiStrong on general fitness measured via the Barthel index in malnourished sarcopenic, adults, aged 60 and above. The trial will incorporate a "Y" design whereby all 75 participants begin on the base formula (MediDrink Platinum) for 2 weeks before being randomised into the SPR-01 alone (n=37, dose calculated per individual but at least 1200 kcal/day) or SP1-01 and PeptStrong (n=38, dose calculated per individual but at least 1200 kcal per day and 2.4g/day, respectively) supplementation arms for 10 weeks. Other clinical endpoints measured as secondary endpoints will include hand grip strength, physical functioning via time up\&go test and changes in fat-free body mass.

Conditions

Interventions

TypeNameDescription
OTHERMediDrink Platinum+MediDrink Platinum+ containing novel protein blend SPR-01
OTHERMediDrink Platinum+ and PeptiStrongMediDrink Platinum+ containing novel protein blend SPR-01 and PeptiStrong, fava bean protein hydrolysate

Timeline

Start date
2025-09-10
Primary completion
2026-10-01
Completion
2027-01-02
First posted
2026-01-07
Last updated
2026-01-07

Locations

2 sites across 1 country: Hungary

Source: ClinicalTrials.gov record NCT07322653. Inclusion in this directory is not an endorsement.