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RECRUITING
NCT07028528
PHASE2

Levagen+ Efficacy Study on Diabetic Peripheral Neuropathy

Sponsor: RDC Clinical Pty Ltd

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to assess the efficacy of Levagen+ supplementation for the symptoms of diabetic peripheral neuropathy (DPN) in patients with DPN. Participants will have remote visits and attend a local pathology centre for blood draws. They will take the study product for 12 weeks, from baseline to week 12 they will have remote visits every 3 weeks.

Official title: A Randomized Placebo Controlled Trial Assessing the Efficacy of Levagen+ for Treating Symptoms of Diabetic Peripheral Neuropathy

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2025-07-01

Completion Date

2026-05

Last Updated

2025-07-23

Healthy Volunteers

No

Interventions

DIETARY_SUPPLEMENT

Levagen+

Participants will take 1 capsule twice daily with water after food. Each capsule will contain: A175mg containing 150 mg of palmitoylethanolamide (PEA). Total daily dose of 350mg Levagen+ containing 300 mg PEA

OTHER

Placebo

Participants will take 1 capsule twice daily with water after food. Each capsule will contain microcrystalline cellulose \[MCC\]

Locations (1)

RDC Clinical

Fortitude Valley, Queensland, Australia