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The effect of cystone on stone expulsion

The effect of cystone on stone expulsion after extracorporeal shock wave lithotripsy: a randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015042221900N1
Enrollment
100
Registered
2016-08-31
Start date
2015-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Kidney and urinary tract stone. N20 Calculus of kidney and ureter - N21 Calculus of lower urinary tract - N22* Calculus of urinary tract in diseases classified elsewhere- N23 Unspecified renal colic

Interventions

Intervention group: Cystone 5 mg oral tablet, twice a day (every 12 hours) from the begining of Lithotripsy until one month.
Intervention 1: Intervention group: Cystone 5 mg oral tablet, twice a day (every 12 hours) from the begining of Lithotripsy until one month. Intervention 2: Control group: Non-use of cystone 5 mg oral
Treatment - Drugs
Control group: Non-use of cystone 5 mg oral tablet

Sponsors

Vice chancellor for Research and Technology, Islamic Azad University of Shahrood
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with kidney stones smaller than 2 cm. Exclusion criteria: history of kidney surgery, Concomitant use of other drugs for treatment of kidney stones; hydronephrosis.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Kidney stone expulsion. Timepoint: Before and one month after intervention. Method of measurement: Abdominal X-ray, CT scan and sonography.

Secondary

MeasureTime frame
Therapy sessions of kidney Lithotripsy. Timepoint: Six months after the first Lithotripsy. Method of measurement: Record number of doing Lithotripsy.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzade khamedi

Islamic Azad University of Shahroud

azadeh.khamedi@yahoo.com+98 23 3223 7331

Outcome results

None listed

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