Use of Alfuzosin in Stone Treatment With ESWL

Sponsor
Singapore General Hospital (Other)
Overall Status
Withdrawn
CT.gov ID
NCT00388271
Collaborator
Sanofi (Industry)
0
1
2
14
0

Study Details

Study Description

Brief Summary

Urinary tract stones may form in the kidneys or along the ureteric tracts and when left untreated, may result in complications such as pain, bleeding, infection and obstruction. ESWL (extra-corporeal shock wave lithotripsy) has been shown to be an effective and safe method of treatment for kidney and ureteric stones in-situ. In our centre, ESWL is done on an outpatient basis with oral pain killers in the weeks following treatment. Patients are also instructed to increase their fluid intake during this period to expedite the clearance of stone fragments. There have been studies to show that pain caused by stones is due to smooth muscle spasm along the ureters, possibly mediated by alpha-receptors. Alpha-blockers have been shown to improve the expulsion of stones and also improve pain relief when used alone, or together with ESWL treatment. In our study, we seek to investigate if alpha-blocker therapy (Alfuzosin) increases stone free rates and improves pain control after ESWL for renal and ureteric stones. The potential benefits include a higher rate of stone clearance and better pain control

Condition or Disease Intervention/Treatment Phase
  • Drug: Alfuzosin (Xatral)
  • Drug: standard treatment
Phase 3

Detailed Description

Urinary tract stones may form in the kidneys or along the ureteric tracts and when left untreated, may result in complications such as pain, bleeding, infection and obstruction. ESWL (extra-corporeal shock wave lithotripsy) has been shown to be an effective and safe method of treatment for kidney and ureteric stones in-situ. In our centre, ESWL is done on an outpatient basis with oral pain killers in the weeks following treatment. Patients are also instructed to increase their fluid intake during this period to expedite the clearance of stone fragments. Alpha1-adrenergic blockers have been shown to improve stone free rates in renal stones and lower ureteric stones. Tamsulosin has been the agent most commonly investigated. There have been no studies done to study the effectiveness of Alfuzosin in stone treatment. Alfuzosin has been shown to be effective in treating benign prostatic hypertrophy, and has a good safety profile. Deliveliotis et al has shown that alfuzosin improves symptoms and quality of life in patients with double-J stents.

This is a prospective, randomised, double-blind, placebo-controlled study involving patients undergoing ESWL for renal and ureteric stones. Exclusion criteria applies (please see below). The patients will be randomised into 2 groups: study VS control. Randomisation is done by using a computer generated list with block randomisation, assigning consecutive patients to either treatment arms. Our standard treatment is intravenous pethidine 50mg and intravenous maxolon 10mg at the onset of the ESWL session, followed by oral analgesics- NSAIDs with a gastroprotective agent. For this study, we will standardise all to oral naproxen 550mg BD with oral omeprazole 20mg BD. The study group will receive the standard treatment, with oral alfuzosin 10mg ON for 1 month, while the control group will receive a placebo. Patients will be given a diary in which to chart their pain scores, use of analgesics, episodes of pain, passage of stones, side-effects of the medications and complications of treatment. At the end of one month, all patients will be called back for review. Stone free status is ascertained with an X-ray, and the diary will be collected for further analysis.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
To Investigate if Alpha-blocker Therapy (Alfuzosin) Increases Stone Free Rates and Improves Pain Control After ESWL (Extra-corporeal Shock Wave Lithotripsy) for Renal and Ureteric Stones.
Study Start Date :
Oct 1, 2006
Actual Primary Completion Date :
Dec 1, 2007
Actual Study Completion Date :
Dec 1, 2007

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 1

xatral

Drug: Alfuzosin (Xatral)
standard treatment plus alfuzosin

Placebo Comparator: 2

standard treatment

Drug: standard treatment
standard treatment

Outcome Measures

Primary Outcome Measures

  1. Reduction in pain score [1 month]

  2. Reduction in use of analgesics [1 month]

  3. stone free rate [1 month]

Secondary Outcome Measures

  1. Severe giddiness as a side-effect [1 month]

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All adult patients referred to our centre for ESWL treatment of renal or ureteric stones who give their informed consent.
Exclusion Criteria:
  • Documented allergy or severe side effects to opioids/ NSAIDs/ Alfuzosin Severe hydronephrosis (on ultrasound or IVU) Radiolucent stones Urinary tract infections Previous pyeloureteral surgery Lower pole stones DJ stents in situ for stones Known renal/hepatic impairment or coagulopathy Pregnant Severe skeletal disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 Urology Centre Singapore Singapore

Sponsors and Collaborators

  • Singapore General Hospital
  • Sanofi

Investigators

  • Principal Investigator: Tsung Wen Chong, MBBS, FRCS, SGH Urology

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Singapore General Hospital
ClinicalTrials.gov Identifier:
NCT00388271
Other Study ID Numbers:
  • SGH/URO/XTR001
First Posted:
Oct 16, 2006
Last Update Posted:
Feb 10, 2017
Last Verified:
Feb 1, 2017
Keywords provided by Singapore General Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 10, 2017