Alfuzosin for Medical Expulsion Therapy of Ureteral Stones
Information source: United States Naval Medical Center, San Diego
Information obtained from ClinicalTrials.gov on February 07, 2013 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Kidney Stones
Intervention: Alfuzosin (Drug); nifedipine (Drug); doxazosin (Drug); prazosin (Drug)
Phase: Phase 3
Status: Recruiting
Sponsored by: United States Naval Medical Center, San Diego Official(s) and/or principal investigator(s): Brian K. Auge, M.D., Principal Investigator, Affiliation: NMCSD Sean P. Stroup, M.D., Principal Investigator, Affiliation: NMCSD
Overall contact: Brian K. Auge, M.D., Phone: 619-532-7200
Summary
The goal of this study is to conduct a prospective controlled trail of four currently
approved Department of Defense (DOD) - formulary medications for use as medical expulsion
therapy (MET) for kidney stones. Between 8% and 15% of Americans will develop symptomatic
urolithiasis in there life. Several medications, including steroids, calcium channel
blockers, alpha-adrenergic antagonists and non-steroidal anti-inflammatory drugs, have been
utilized to aid in the spontaneous passage of distal ureteral calculi. Recently, use of
selective alpha-blockers has shown promise for medical expulsion therapy (MET) of distal
ureteral calculi. None of these studies have been widely publicized outside the specialty of
urology. Recent studies have shown a success rate of nearly 90% when the selective
alpha-blocker tamsulosin (Flomax) was used for MET. MET has also been shown to result in a
decreased narcotic requirement, shorter time to stone passage, and reduced requirement for
further interventions. The investigators will evaluate the effectiveness of MET as initial
management for kidney stones using DOD-approved formulary medications.
Clinical Details
Official title: Evaluation of Alfuzosin as Medical Expulsion Therapy for Ureteral Stones
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: The primary measures are percent of stones passed and rates of occurrence of various side effects (categorical variables), and time to pass, pain scale, and amount of pain medication taken (continuous variables).
Detailed description:
Patients presenting to Naval Medical Center San Diego with symptomatic ureteral stones
visible on CT and KUB, and who are medically stable will be offered enrollment. Upon
consent, patients will be randomly assigned to one of four outpatient treatment arms,
randomized 1: 1:1: 1 and include; Group 1 - Alfuzosin 10 mg daily, Group 2 - Nifedipine 30 mg daily, Group 3 - Doxazosin 4 mg daily, or Group 4 - Prazosin 1 mg twice daily. The primary
endpoint is stone expulsion rate and secondary endpoints are time to expulsion, need for
additional intervention, degree of pain control, amount of narcotic use, and evaluation of
study drug side effects. The treatment regimens consist of daily medication until the stone
passes or 21 days, whatever is shorter. Patients will also receive oral pain medication as
needed.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Age >/= 18 years
- Single ureteral stone < 1 cm in greatest dimension
Exclusion Criteria:
- Age < 18 years
- Active unstable angina
- History of or active postural hypotension (>20 mmHg drop in orthostatic SBP)
- Allergy to alpha-blockers
- Acute or Chronic Renal Failure as demonstrated by a serum creatinine of > 1. 4 mg/dl
- Urinary tract infection
- Multiple ureteral stones
- Current uncontrolled diabetes
- Alpha-blocker therapy within 30 days for any reason
- Current pregnancy or lactation
- Patient desire for immediate stone removal
Locations and Contacts
Brian K. Auge, M.D., Phone: 619-532-7200
Naval Medical Center San Diego, San Diego, California 92134, United States; Recruiting Brian K Auge, M.D., Phone: 619-532-7200 Sean P. Stroup, M.D., Phone: 619-532-7200 Brian K. Auge, M.D., Principal Investigator Sean P. Stroup, M.D., Principal Investigator
Additional Information
Starting date: January 2008
Last updated: April 25, 2012
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