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NCT03052062

Tolerance Study of the Dietary Supplement Lipidrive (ECPH1-03)

Completed Phase 1, PHASE2 Last updated 6 July 2018
What this trial tests

Phase 1, PHASE2 trial testing Lipidrive in Obese in 20 participants. Completed in 3 July 2018.

Timeline
2 March 2017
Primary endpoint
3 July 2018
3 July 2018

Quick facts

Lead sponsorValbiotis
PhasePhase 1, PHASE2
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date2 March 2017
Primary completion3 July 2018
Estimated completion3 July 2018
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Valbiotis

Who can join

Adults 45 to 65, male only, with Obese. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objectives of this clinical study are to determine the tolerance of dietary supplement Lipidrive through the evaluation of several parameters : * Various blood biological parameters * Urinary parameters * Hemodynamic indicators * Cardiac function * Anthropometric variables

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Poster abstracts
    · 2018

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Other recruiting trials for Obese

Currently open trials in the same condition.

Other Valbiotis 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/NCT03052062.

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