Clinical Efficacy Trial of Burdock Root Extract in Patients With Asymptomatic Hyperuricaemia
Key facts
- Where
- Kyiv, UkraineSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 35 and 65 years old?
Source: NCT07002762, who can take part
Where in Ukraine
- State Institution "National Research Centre "Academician M. D. Strazhesko Institute of CardiologyKyiv, UkraineContact: Valentin ShichkinTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- OMNIFARMA LLC
- Trial code
- NCT07002762
- Record updated
- 30 July 2025
- Original description
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 placeboRead full original descriptionShow less
Multicentre, Double-blind, Randomized, Placebo-controlled Trial of Clinical Efficacy of Burdock Root Extract in Patients With Asymptomatic Hyperuricaemia
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
Inclusion: 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; Women of reproductive age having negative pregnancy test at the baseline and at the end of the trial; Not taking any diuretics, or their administration based on a regimen usual for a patient, without changes; Not taking part in any other clinical trials; Consent and voluntarily signed informed consent form for participation in the clinical trial.
Exclusion: Patients with any somatic evidences of hyperuricaemia including gout taking antigout drugs during or within 6 months before the trial; Presence of any concomitant decompensated diseases or acute conditions able to influence results of the trial; Alcohol abuse and drug addiction; Changes in taking diuretics within a month before and during the trial; Patients with mental disorders / taking antipsychotics or antidepressants; Age <35 or >65 years; Fever (above 36.8 оС); Pregnancy and lactation; Patients not giving (informed) consent to participate in the trial; Patients causing doubts of the study doctor as to their motivation to comply with the trial; Participation in any other clinical trial; Taking any nutritional additives.