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The effect of tamsulosin on ureteral stones expulsion

Effect of tamsulosin on lower ureteral stone expulsion

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016012626211N1
Enrollment
100
Registered
2016-05-25
Start date
2016-04-13
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 stone. Calculus of ureter

Interventions

Intervention 1: Intervention: Oral tamsulosin 4 mg Intervention method: Prescribed tamsulosin Morning, and for prescribing it until the stone is Or in case of expulsion for up to four weeks after in
Treatment - Drugs
Control:Non-use of tamsulosin oral 4mg Control Method: All patients from both groups to allow the use of 100 mg indomethacin treatment for symptomatic PRN (in case of unbearable pain) is given. All
Intervention: Oral tamsulosin 4 mg Intervention method: Prescribed tamsulosin Morning, and for prescribing it until the stone is Or in case of expulsion for up to four weeks after initiation of the

Sponsors

adjutancy of Research and Technology, Islamic Azad University of Shahrood
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for the project: Patients between the ages of 18 and 60 years in with renal colic with 3 to 6 mm stones in distal ureteral or ureteral uvj Exclusion criteria: UTI; Radiolucent stones on KUB; sever Hydronephrosis (grades 2 and 3 in ultrasound; Diabetes (FBS more than 125 milligrams per deciliter); history of peptic ulcer disease; Systolic blood pressure less than 100 mm Hg; Consumers calcium antagonist drugs; history of surgery on the distal ureter; single kidney ; creatinine more than 1.4 mg per deciliter in men and 1.2 in women; Intractable pain; NSAID intolerance ; side effects of tamsulosin; pregnancy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Stone expulsion rate. Timepoint: 4 weeks after treatment. Method of measurement: Questionnaire.;Stone expulsion time. Timepoint: 4 weeks after treatment. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Amount of sedative. Timepoint: 4 weeks after treatment. Method of measurement: Questionnaire.;Drug side effects. Timepoint: 4 weeks after treatment. Method of measurement: Questionnaire.;Stone complications. Timepoint: 4 weeks after treatment. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaghme Ahi

Islamic Azad University of Shahroud

N-Ahi@iau-shahrood.ac.ir+98 23 3239 0077

Outcome results

None listed

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