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Rudioretic supplement and kidney stone

Evaluation of the effect of Rudioretic supplement comparing to placebo on renal stone: A randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140804018677N12
Enrollment
160
Registered
2021-08-17
Start date
2021-09-11
Completion date
Unknown
Last updated
2021-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kidney stone. Calculus of kidney

Interventions

Intervention 1: Supplement group A: will receive 2 capsules of Rudioretic every 8 hours with empty stomach for 6 weeks. Each capsule contain 500 mg of Zea mays, Apium graveolens, Equisetum arvense and

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Diagnosed with a kidney stone without hydronephrosis and no need for medication Age between 18-45 years Willing to participate in the study

Exclusion criteria

Exclusion criteria: Pregnancy or lactation Having known heart disease Receiving drugs that affect kidney stones

Design outcomes

Primary

MeasureTime frame
Number of excreted kidney stone. Timepoint: Start of intervention and a month later. Method of measurement: Ultrasonography and blood and urine tests.;Stone size. Timepoint: Start of intervention and a month later. Method of measurement: Sonography.

Secondary

MeasureTime frame
Urine volume 24 h. Timepoint: Start of intervention and a month later. Method of measurement: Urine 24 h test by BT-1500 autoanalyser.;Creatinine in urine 24h. Timepoint: Start of intervention and a month later. Method of measurement: Urine 24h test by Pars Azmoon kit.;Oxalate in urine 24 h. Timepoint: Start of intervention and a month later. Method of measurement: urine 24 h test by Darmankau kit.;Citrate in urine 24 h. Timepoint: Start of intervention and a month later. Method of measurement: urine 24 h test by Darmankau kit.;Uric acid in urine 24 h. Timepoint: Start of intervention and a month later. Method of measurement: urine 24h test by Pars Azmoon kit.;Urine specific gravity. Timepoint: Start of intervention and a month later. Method of measurement: Urinalysis by BT-1500 autoanalyser.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoodeh Razghei Jahromi

Shahid Beheshti University of Medical Sciences

soodehrazeghi@gmail.com+98 21 2235 7483

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026