To study the efficacy of extended-release Urocitra in patients with observing intact pills in feces

To study the efficacy of Extended-release Urocitra on urinary pH and 24-hour urine citrate in patients with observing the intact pills in feces without chronic diarrhea

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20191026045244N4

Enrollment

Registered

2022-08-17

Start date

2022-04-21

Completion date

Unknown

Last updated

2022-08-29

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

Conditions

Renal stone. Encounter for examination for normal comparison and control in clinical research program

Interventions

Intervention 1: Intervention group: Patients with prevous history of observing the intact pills of Extended-release Urocitra in feces (without chronic diarrhea), will treated by potassium citrate ext

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Urolithiasis patients with and without observing extended release Urocitra in feces

Exclusion criteria

Exclusion criteria: chronic kidney disease (stage 3&4) pregnancy or lactation

Design outcomes

Primary

Measure	Time frame
24-hour urine citrate. Timepoint: after 4 weeks treatment with Extended-release Urocitra. Method of measurement: 24- hour urine citrat measurment (enzymatic), mg/day.;Urine pH. Timepoint: after 4 weeks treatment with Extended-release Urocitra. Method of measurement: Measurement of fresh urine pH by pH meter.;Investigation of the possibility of recurrence of observing intact pills in the feces of patients with previous proclem. Timepoint: After four weeks. Method of measurement: Questionnaire.	—

Measure

Time frame

24-hour urine citrate. Timepoint: after 4 weeks treatment with Extended-release Urocitra. Method of measurement: 24- hour urine citrat measurment (enzymatic), mg/day.;Urine pH. Timepoint: after 4 weeks treatment with Extended-release Urocitra. Method of measurement: Measurement of fresh urine pH by pH meter.;Investigation of the possibility of recurrence of observing intact pills in the feces of patients with previous proclem. Timepoint: After four weeks. Method of measurement: Questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbbas Basiri

Shahid Beheshti University of Medical Sciences

basiri@unrc.ir+98 21 2256 7222

Outcome results

None listed

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