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Differential Effect of Silodosin Versus Tamsulosin on Stone Clearance After Extra-corporeal Shock Wave Lithotripsy

A

Albert Einstein Healthcare Network

Status and phase

Withdrawn
Phase 3

Conditions

Kidney Stones

Treatments

Procedure: Extra-corporeal shock wave lithotripsy
Drug: Tamsulosin
Drug: silodosin

Study type

Interventional

Funder types

Other

Identifiers

NCT01560091
HN 4378

Details and patient eligibility

About

Tamsulosin is an alpha blocker usually prescribed for urinary complaints that has been shown to have some benefit in allowing kidney stones to pass through the ureter. Silodosin is a new alpha blocker that acts more rapidly than tamsulosin and has been shown to have specific receptors on the ureter. The investigators would like to see if there is some benefit to taking silodosin over tamsulosin after extra-corporeal shock wave lithotripsy (ESWL) to break kidney stones in terms of allowing the ureteral fragments to pass through the ureter. Our hypothesis is that silodosin will be at least as effective as tamsulosin in terms of allowing stones to pass, but may allow them to pass more quickly because of the rapid onset of action.

The side effect profile for both drugs is quite similar and tolerable. Patients may experience some common side effects associated with tamsulosin, including abnormal ejaculation, dizziness, rhinitis (runny nose, sneezing), and somnolence (sleepiness). Serious reactions include orthostatic hypotension, syncope (fainting), and priapism (prolonged undesired erection).

Patients may experience some common side effects with both silodosin and tamsulosin including ejaculatory dysfunction, dizziness, postural hypotension, diarrhea, and headache. Serious side effects are rare and include orthostatic hypotension, intra-operative floppy iris syndrome, syncope, and priapism.

Patients will experience the discomfort normally associated with kidney stones. All efforts will be made to alleviate these discomforts, including the use of the study medications. Patients will be able to take their routine prescribed pain medications, and will be asked to keep a record of their pain medication use.

The investigators will be randomly enrolling patients from all racial backgrounds and of both genders. They must have kidney stones ranging in size from 4mm to 1.0 cm and have no prior treatment for the study.

The primary endpoint of this study is the clearance rate of kidney stones. That is, in what period of time does the patient achieve clearance, is stone free and has all residual stones gone. The secondary endpoints of this study include analgesic use, residual stones remaining, need for re-treatment, need for intervention, steinstrasse clearance, and the need for hospitalization.

Full description

A comparison between two commonly used alpha blockers to determine if there is superiority in the secondary usage of aiding in stone passage

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults age 18 to 70
  • Non-diabetics
  • White blood cell count and serum creatinine level within normal range
  • Urine analysis consistent with absence of infection
  • Negative urine culture
  • Absence of subjective or objective fever
  • Ability to tolerate oral fluids and pain medication
  • Unilateral ureteral calculus < 10mm visible on CT scan within the ureter
  • Ability to make informed medical decisions regarding consent
  • Willingness to follow up in the urology office

Exclusion criteria

Adults unable to consent

  • Individuals who are not yet adults (infants, children, teenagers)
  • Pregnant women
  • Prisoners
  • Prior treatment for this particular stone
  • Medical therapy only for stone disease
  • Chronic narcotic use
  • Current alpha blocker therapy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 3 patient groups, including a placebo group

Group A
Placebo Comparator group
Description:
Patients will receive ESWL and no medication
Treatment:
Procedure: Extra-corporeal shock wave lithotripsy
Group B
Active Comparator group
Description:
Patients will receive Flomax after ESWL
Treatment:
Procedure: Extra-corporeal shock wave lithotripsy
Drug: Tamsulosin
Group C
Active Comparator group
Description:
Patients will receive silodosin after ESWL
Treatment:
Procedure: Extra-corporeal shock wave lithotripsy
Drug: silodosin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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