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Completed

NCT Number: NCT00382265

Tamsulosin for Urolithiasis in the Emergency Dept

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of Alabama - Birmingham, Birmingham, Alabama, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Tamsulosin

Drug

tamsulosin 0.4mg po qd for 28 days

Placebo

Other

placebo po qd for 28 days

Primary outcomes

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

    Time frame: 28 days

    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.

Secondary outcomes

  1. Any Pain Medication

    Time frame: 28 days

    Patients on any pain medication at day 28

  2. Need for Surgical Intervention

    Time frame: 28 days

  3. Crossover to Open Label Tamsulosin

    Time frame: 28 days

  4. Confirmation of Stone Passage on CT

    Time frame: 28 days

  5. Return to Work (if Employed)

    Time frame: 28 days

Sponsors and collaborators

Lead sponsor

Andrew Meltzer

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Official study title

Study of Tamsulosin for Urolithiasis in the Emergency Department

Acronym: STONE

Important dates

Study start
2008
Primary completion
2017
Study completion
2017
First posted
Sep 29, 2006
Registry last updated
Dec 10, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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