Burdock Root (Arctium lappa) trials recruiting now

1 registration that name burdock Root as a study arm and are recruiting or about to, as ClinicalTrials.gov listed them on Oct 20, 2026. Read each listing for its full criteria and current status.

Kymata never assesses eligibility. Each listing names its own criteria; only its study team can say whether someone can join. Trial doses are given under the trial's monitoring and are not a schedule for anyone outside it.

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All 1 registrations

RecruitingNCT07002762

Clinical Efficacy Trial of Burdock Root Extract in Patients With Asymptomatic Hyperuricaemia

  • No phase
  • OMNIFARMA LLC
  • About 100 people
  • Started Mar 12, 2025

In plain words A study of burdock Root in people 35 to 65, run by OMNIFARMA LLC. It plans to enroll about 100 people at 1 site, none in the US.

Who it lists and where

Who the trial lists, as registered

Lists people 35 to 65. Conditions: Hyperuricemia or Gout.

  • Hyperuricaemia confirmed by a laboratory, uric acid level from 360 to 540 μmol/L in women and from 420 to 540 μmol/L in men;
  • Age from 35 to 65 years at the baseline;
  • Patients examined by an experienced specialist not revealing any clinical evidences of gout or other somatic consequences of hyperuricaemia;
  • Not taking any other nutritional additives;

4 more inclusion criteria and the exclusion criteria are on the listing.

What it tests, as registered

Burdock ( Arctium lappa L.) root extract in a form of a nutritional additive; Placebo

Registered summary

Multicentre, double-blind, randomized, placebo-controlled trial of the clinical efficacy of burdock root extract in patients with asymptomatic hyperuricemia, with the primary objective to assess the efficacy of the use of burdock root extract in patients with asymptomatic hyperuricaemia versus placebo

Where, as registered

No US site; Ukraine (1).

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