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Tamsulosin for Urolithiasis in the Emergency Dept

Study of Tamsulosin for Urolithiasis in the Emergency Department

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00382265
Acronym
STONE
Enrollment
512
Registered
2006-09-29
Start date
2008-01-31
Completion date
2017-02-01
Last updated
2018-12-10

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

Conditions

Ureterolithiases

Keywords

urolithiasis, renal colic, kidney stones, urinary stone disease

Brief summary

Urolithiasis is a disease that effects 12% of the population and its incidence is growing. In the US there are over 1.1 million visits annually to Emergency Departments for renal colic. The disease is extremely painful, often requiring large amounts of narcotic analgesia, and results in lost work days. Moreover, up to 30% of patients may eventually require lithotripsy or surgical removal of the stone. Currently there are no medical interventions other than analgesia which are offered to patients. Based on encouraging results from several small European clinical studies, the researchers hypothesize that the administration of tamsulosin to patients with symptomatic urolithiasis will enhance stone passage, and reduce both the time to recovery and the need for surgical intervention or lithotripsy. The researchers will conduct a study by identifying and recruiting patients presenting with urolithiasis in the emergency departments of four institutions. A total of 500 consenting subjects will be randomly assigned to one of two groups: 1. tamsulosin for a maximum of 28 days; 2. placebo for a maximum of 28 days. In addition, both groups will receive standard analgesic therapy. The study team, which will be blinded to treatment status, will monitor each subject's clinical progress and outcome. The primary objectives of this study are: 1. to determine if tamsulosin is effective, and 2. to evaluate the safety of the therapy. Another objective is to identify the most appropriate clinical subgroup(s) for treatment. If the therapeutic benefits observed in smaller clinical studies are replicated, administration of these medications should produce several benefits, including: 1. a reduction in time to pain free recovery and hence a more rapid return to employment; 2. decreased requirements for narcotic analgesia; 3. less need for urological out-patient clinic follow-up; 4. decreased need for surgical intervention or lithotripsy; and 5. substantial cost savings. If this therapy is beneficial, it will represent a major advance in the treatment of urolithiasis. This objective is a major stated goal of the NIDDK (National Institute of Diabetes and Digestive and Kidney Diseases) Clinical Urology Program, which has a stated mission to improve the treatment of urolithiasis. Kidney stones are a major public health issue, and one person in eight will be affected by the disease. If the hypothesis is verified, the researchers will provide the first medical therapy ever for this disease. This therapy, if effective, will reduce the amount of time a patient is off work because of the pain from the disease, and may also reduce the need for expensive and time-consuming surgical treatments.

Interventions

DRUGtamsulosin

tamsulosin 0.4mg po qd for 28 days

OTHERPlacebo

placebo po qd for 28 days

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
Andrew Meltzer
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age ≥ 18 years 2. Evidence of ureterolithiasis (i.e. stone is located in ureter, not in bladder) as demonstrated on radiographic studies, specifically non-contrast spiral CT. 3. Willingness to participate and able to proceed with standard outpatient management (no personal or job-related issues, e.g. airline pilot. 4. Has a telephone in order to be contacted for follow-up.

Exclusion criteria

1. Patient desiring or requiring immediate surgical intervention making then not a candidate for outpatient kidney stone management. 2. Current urinary tract infection based on urine dipstick as admission and urgent procedural management are likely indicated. 3. Known anatomical genitourinary abnormalities or prior Genitourinary surgeries. 4. Positive pregnancy test making proper radiological imaging contraindicated. 5. Breastfeeding mothers. 6. History of hypersensitivity to tamsulosin. 7. Current use of alpha blockers or calcium channel blockers. 8. Current use of steroids which may have an independent effect on stone expulsion. 9. Spontaneous stone expulsion prior to enrollment. 10. Largest stone dimension ≥ 9mm assessed using radiologic imaging, being very unlikely to pass spontaneously. 11. Presence of stone in the bladder. 12. Current use of vardenafil which is tamsulosin contraindicated. 13. Ipsilateral, transplanted or solitary kidney as hospitalization may be necessary. 14. Known renal insufficiency. 15. Fever defined as \>101.5°F which may indicate infection. 16. Floppy iris syndrome which is tamsulosin contraindicated. 17. Planned cataract surgery in the next 60 days which is tamsulosin contraindicated. 18. Prisoners /wards of state. 19. Prior enrollment in STONE (Candidates who are screened and found ineligible may be rescreened at a later date.)

Design outcomes

Primary

MeasureTime frameDescription
Proportion of Patients Passing Their Stone Within 28 Days by Self Report28 daysHypothesis: The administration of tamsulosin after the clinical and radiographic diagnosis of acute urolithiasis will produce an increase in the proportion of patients passing their stone within 28 days.

Secondary

MeasureTime frameDescription
Any Pain Medication28 daysPatients on any pain medication at day 28
Need for Surgical Intervention28 days
Crossover to Open Label Tamsulosin28 days
Confirmation of Stone Passage on CT28 days
Return to Work (if Employed)28 days

Countries

United States

Participant flow

Participants by arm

ArmCount
Tamsulosin Group
Tamsulosin 0.4mg PO tamsulosin: tamsulosin 0.4mg po qd for 28 days
267
Placebo Group
Placebo for 28 days
245
Total512

Baseline characteristics

CharacteristicTamsulosin GroupPlacebo GroupTotal
Age, Continuous41.8 years
STANDARD_DEVIATION 13.6
39.3 years
STANDARD_DEVIATION 12.9
40.6 years
STANDARD_DEVIATION 13.3
Race/Ethnicity, Customized
Non-White Race
56 Participants54 Participants110 Participants
Region of Enrollment
United States
267 participants245 participants512 participants
Sex: Female, Male
Female
70 Participants69 Participants139 Participants
Sex: Female, Male
Male
197 Participants176 Participants373 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 2670 / 245
other
Total, other adverse events
0 / 2670 / 245
serious
Total, serious adverse events
0 / 2670 / 245

Outcome results

Primary

Proportion of Patients Passing Their Stone Within 28 Days by Self Report

Hypothesis: The administration of tamsulosin after the clinical and radiographic diagnosis of acute urolithiasis will produce an increase in the proportion of patients passing their stone within 28 days.

Time frame: 28 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
TamsulosinProportion of Patients Passing Their Stone Within 28 Days by Self Report128 Participants
PlaceboProportion of Patients Passing Their Stone Within 28 Days by Self Report113 Participants
Secondary

Any Pain Medication

Patients on any pain medication at day 28

Time frame: 28 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
TamsulosinAny Pain Medication22 Participants
PlaceboAny Pain Medication24 Participants
Secondary

Confirmation of Stone Passage on CT

Time frame: 28 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
TamsulosinConfirmation of Stone Passage on CT102 Participants
PlaceboConfirmation of Stone Passage on CT90 Participants
Secondary

Crossover to Open Label Tamsulosin

Time frame: 28 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
TamsulosinCrossover to Open Label Tamsulosin15 Participants
PlaceboCrossover to Open Label Tamsulosin14 Participants
Secondary

Need for Surgical Intervention

Time frame: 28 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
TamsulosinNeed for Surgical Intervention14 Participants
PlaceboNeed for Surgical Intervention13 Participants
Secondary

Return to Work (if Employed)

Time frame: 28 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
TamsulosinReturn to Work (if Employed)202 Participants
PlaceboReturn to Work (if Employed)185 Participants

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026