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NCT04684771

Tolerance, Efficacy, revAlidation, Myostim

Completed NA Last updated 28 December 2020
What this trial tests

NA trial testing MYOSTIM® in Anterior Cruciate Ligament Rupture in 35 participants. Completed in 31 December 2017.

Timeline
23 March 2015
Primary endpoint
27 July 2017
31 December 2017

Quick facts

Lead sponsorAlternativa International S.A
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposesupportive care
Enrollment35
Start date23 March 2015
Primary completion27 July 2017
Estimated completion31 December 2017
Sites2 locations across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Alternativa International S.A

Who can join

Adults 18 to 40, any sex, with Anterior Cruciate Ligament Rupture. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Evaluation of efficacy and tolerance of a food supplement (MYOSTIM®) versus a placebo in postoperative revalidation of patients after reconstructive surgery of anterior cruciate ligament. The food supplement (MYOSTIM®) has been developped and is supplied as food bars and composed of pomegranate, leucine, creatine, proteins and D vitamin. The aim of this exploratory study is to assess the efficacy and tolerance of MYOSTIM® on muscle performance after ACL reconstructive surgery and in postoperative revalidation phase.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Anterior Cruciate Ligament Rupture

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04684771.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing