Tamsulosin for Urolithiasis in the Emergency Dept (STONE)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2011 by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ClinicalTrials.gov Identifier:
NCT00382265
First received: September 28, 2006
Last updated: February 4, 2011
Last verified: February 2011

September 28, 2006
February 4, 2011
January 2008
August 2010   (final data collection date for primary outcome measure)
The proportion of patients passing their stone at 28 days [ Time Frame: 28 days ] [ Designated as safety issue: No ]
Not Provided
Complete list of historical versions of study NCT00382265 on ClinicalTrials.gov Archive Site
Time to passage of stone Length of time in pain Number of days lost from work Need for surgical intervention or lithotripsy Overall costs [ Time Frame: 28 days ] [ Designated as safety issue: No ]
Not Provided
Not Provided
Not Provided
 
Tamsulosin for Urolithiasis in the Emergency Dept
Study of Tamsulosin for Urolithiasis in the Emergency Department

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 302 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.

The secondary 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 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.

Not Provided
Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Nephrolithiasis
Drug: tamsulosin
tamsulosin 0.4mg po qd for 28 days
  • Active Comparator: 1
    Tamsulosin 0.4mg PO
    Intervention: Drug: tamsulosin
  • Placebo Comparator: 2
    Placebo
    Intervention: Drug: tamsulosin
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
302
Not Provided
August 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Age > 18
  • Evidence of urolithiasis
  • Acceptable for outpatient stone management

Exclusion Criteria:

  • Urinary tract infection
  • Known anatomical genitourinary (GU) abnormalities, or prior GU surgeries
  • Diabetes
  • Ulcer disease
  • Osteoporosis
  • Pregnancy
  • Psychiatric disorder
  • History of hypersensitivity to tamsulosin or corticosteroids
  • Spontaneous stone expulsion in the ED
  • Largest stone dimension .9mm
  • Concurrent use of vardenafil (Levitra)
  • Solitary kidney
  • Transplanted kidney
  • Renal insufficiency
  • Fever
  • Prisoners or wards of state
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00382265
DK71603 (completed)
Not Provided
Jeremy Brown, MD, The George Washington University Medical Center
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Not Provided
Principal Investigator: Jeremy Brown, MD The George Washington University
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
February 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP