Last reviewed · How we verify

NCT04371237

Accelerating Post-exercise Muscle Glycogen Resynthesis in Humans: Impact of Combined Nutrient Intake and Intermittent Pneumatic Compression or Heat Therapy

Completed NA Last updated 10 March 2021
What this trial tests

NA trial testing Compression sleeve in Muscle Recovery in 26 participants. Completed in 21 December 2019.

Timeline
19 September 2018
Primary endpoint
21 December 2019
21 December 2019

Quick facts

Lead sponsorPepsiCo Global R&D
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposebasic science
Enrollment26
Start date19 September 2018
Primary completion21 December 2019
Estimated completion21 December 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

PepsiCo Global R&D — full company profile →

Who can join

Adults 18 to 35, any sex, with Muscle Recovery or Muscle Soreness. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To determine if modalities designed to improve blood flow combined with post-exercise nutrient intake will improve replenishment of muscle glycogen better than nutrient intake alone. A secondary objective is to compare the effectiveness of heat therapy and intermittent pneumatic compression on glycogen replenishment.

Publications & conference data

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

Verify or expand the search:

Other trials of Compression sleeve

Trials testing the same drug.

Other recruiting trials for Muscle Recovery

Currently open trials in the same condition.

Other PepsiCo Global R&D trials

Trials by the same sponsor.

Verify against primary sources

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/NCT04371237.

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