Tamsulosin as Adjunctive Therapy After Extracorporeal Shock Wave Lithotripsy for Renal Stones
Primary Purpose
Renal Stone
Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Extracorporeal shock wave lithotripsy
Diclofenac
Tamsulosin
Sponsored by
About this trial
This is an interventional treatment trial for Renal Stone focused on measuring Extracorporeal shock wave lithotripsy, Tamsulosin, Urolithiasis
Eligibility Criteria
Inclusion Criteria:
- A single radiopaque kidney stone (5-20 mm) in diameter visible on CT scan of the abdomen.
Exclusion Criteria:
- A lower calyx stone.
- A history of spontaneous stone passage.
- A previous failed ESWL.
- Treatment with alpha adrenergic antagonists, calcium channel inhibitors or steroids.
- Severe obesity (BMI≥40).
- Pregnancy.
- Serum creatinine ≥2 mg/dl.
- Renal artery aneurysm and/or abdominal aorta aneurysm.
- The presence of a ureteral stent.
- Anatomical abnormalities or previous surgery on the upper urinary tract.
- Bone deformities.
- Presence of a urinary tract infection.
- Coagulation disorders.
- Poorly controlled hypertension.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Tamsulosin
Control
Arm Description
At the end of the ESWL session, the patients received standard treatment for analgesia consisting of oral diclofenac (75 mg/12 h) as needed plus oral tamsulosin (0.4 mg/day) for eight weeks.
At the end of the ESWL session, the patients received standard treatment for analgesia consisting of oral diclofenac (75 mg/12 h) as needed
Outcomes
Primary Outcome Measures
Stone-free rate
Percentage of patients with the absence of residual stones (≥ 5 mm in diameter), with the presence of asymptomatic nonsignificant residual stone fragments (≤4 mm in diameter) determined via abdominal computed tomography scan, and with the absence of additional procedures to resolve an event of acute symptomatic urinary obstruction.
Secondary Outcome Measures
Complications rate associated with residual stone fragments
Percentage of patients with the presence of complications associated with residual stone fragments.
Full Information
NCT ID
NCT04819828
First Posted
March 25, 2021
Last Updated
March 26, 2021
Sponsor
Hospital Regional de Alta Especialidad del Bajio
1. Study Identification
Unique Protocol Identification Number
NCT04819828
Brief Title
Tamsulosin as Adjunctive Therapy After Extracorporeal Shock Wave Lithotripsy for Renal Stones
Official Title
Tamsulosin as Adjunctive Therapy After Extracorporeal Shock Wave Lithotripsy for Renal Stones
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
January 1, 2010 (Actual)
Primary Completion Date
August 31, 2016 (Actual)
Study Completion Date
December 31, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Regional de Alta Especialidad del Bajio
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Urolithiasis is a common health problem worldwide affecting approximately 10% of the population at some stage in their lives. The aim of this study is to evaluate the efficacy of adjuvant treatment with tamsulosin for improving the stone-free rate after a single session of extracorporeal shock wave lithotripsy (ESWL) in the treatment of radiopaque kidney stones.
Detailed Description
Urolithiasis is a common health problem worldwide affecting ∼10% of the population at some stage in their lives. It affects approximately 5% of women and 12% of men in the United States, and it has been suggested that the incidence is increasing. Because of its efficacy and low morbidity, extracorporeal shock wave lithotripsy (ESWL) is an effective treatment for kidney stones smaller than 20 mm in diameter. The objective of this therapy is to achieve an adequate fragmentation of the calculus that allows a spontaneous expulsion of the fragments, and finally, a stone-free state, which is not always possible.
The presence of adrenergic receptors in the ureter has suggested the involvement of the sympathetic nervous system in its peristaltic activity. It has also been shown that alpha 1 adrenergic antagonist medications such as tamsulosin are capable of inhibiting the basal tone and the ureteral peristalsis, causing dilation and facilitating the migration of stones. Some authors have reported the efficacy of this type of medication for spontaneous calculus expulsion, but there is no conclusive evidence of the adjuvant effectiveness of tamsulosin after ESWL for stone clearance and even less among a Mexican population.
This is a single center, randomized, non-placebo-controlled study with a sample of adults (men and women ≥18 years old) with a single radiopaque kidney stone (5-20 mm) in diameter. Post-ESWL session, the patients will be randomly divided into two groups (the control group and the tamsulosin group). After discharge, all patients will be instructed to drink a minimum of 2 L water daily. The control group will receive standard treatment for analgesia consisting of oral diclofenac (75 mg/12 h) as needed. The tamsulosin group will receive standard treatment for analgesia plus oral tamsulosin (0.4 mg/day) for eight weeks.
Patients will attend follow-up visits every two weeks during the first month of treatment and a final visit at the end of the second month. During each visit, vital signs will be taken, a physical examination will be conducted, and possible adverse effects will be monitored; additionally, a plain X-ray of the kidney, ureter, and bladder (KUB) will be taken at two and four weeks for evaluating possible complications associated with residual fragments, as well as an abdominal CT scan at eight weeks after the ESWL in order to determine stone-free status.
Data will be analyzed using R Statistical Software. Descriptive statistics will be determined for the patients' clinical characteristics, grouped by the treatment assigned (control group and tamsulosin group) and will be compared using the Mann-Whitney U test or the chi-square test depending on the variable type. The strength of the association between the ESWL treatment with adjuvant tamsulosin and the stone-free rate will be evaluated by calculating the relative risk (RR) and the number needed to treat (NNT). In all cases, an alpha=0.05 was considered significant.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Stone
Keywords
Extracorporeal shock wave lithotripsy, Tamsulosin, Urolithiasis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Tamsulosin
Arm Type
Experimental
Arm Description
At the end of the ESWL session, the patients received standard treatment for analgesia consisting of oral diclofenac (75 mg/12 h) as needed plus oral tamsulosin (0.4 mg/day) for eight weeks.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
At the end of the ESWL session, the patients received standard treatment for analgesia consisting of oral diclofenac (75 mg/12 h) as needed
Intervention Type
Procedure
Intervention Name(s)
Extracorporeal shock wave lithotripsy
Intervention Description
A single session of extracorporeal shock wave lithotripsy: the session will be finished upon reaching a maximum of 4,000 shocks or if a complete fragmentation of the kidney stone is observed.
Intervention Type
Drug
Intervention Name(s)
Diclofenac
Intervention Description
Standard treatment for analgesia: oral diclofenac (75 mg/12 h) as needed.
Intervention Type
Drug
Intervention Name(s)
Tamsulosin
Intervention Description
Oral tamsulosin (0.4 mg/day) for eight weeks.
Primary Outcome Measure Information:
Title
Stone-free rate
Description
Percentage of patients with the absence of residual stones (≥ 5 mm in diameter), with the presence of asymptomatic nonsignificant residual stone fragments (≤4 mm in diameter) determined via abdominal computed tomography scan, and with the absence of additional procedures to resolve an event of acute symptomatic urinary obstruction.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Complications rate associated with residual stone fragments
Description
Percentage of patients with the presence of complications associated with residual stone fragments.
Time Frame
2, 4, and 8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
A single radiopaque kidney stone (5-20 mm) in diameter visible on CT scan of the abdomen.
Exclusion Criteria:
A lower calyx stone.
A history of spontaneous stone passage.
A previous failed ESWL.
Treatment with alpha adrenergic antagonists, calcium channel inhibitors or steroids.
Severe obesity (BMI≥40).
Pregnancy.
Serum creatinine ≥2 mg/dl.
Renal artery aneurysm and/or abdominal aorta aneurysm.
The presence of a ureteral stent.
Anatomical abnormalities or previous surgery on the upper urinary tract.
Bone deformities.
Presence of a urinary tract infection.
Coagulation disorders.
Poorly controlled hypertension.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rafael E Maldonado-Valadez, MD, MSc
Organizational Affiliation
Hospital Regional de Alta Especialidad del Bajio
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Edel R Rodea-Montero, MPH
Organizational Affiliation
Hospital Regional de Alta Especialidad del Bajio
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jose A Alvarez-Canales, MD, Phd
Organizational Affiliation
Hospital Regional de Alta Especialidad del Bajio
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Angel D Valdez-Vargas, MD
Organizational Affiliation
Hospital Regional de Alta Especialidad del Bajio
Official's Role
Study Chair
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35685573
Citation
Maldonado-Valadez RE, Valdez-Vargas AD, Alvarez JA, Rodea-Montero ER. Efficacy of Adjuvant Tamsulosin for Improving the Stone-Free Rate after Extracorporeal Shock Wave Lithotripsy in Renal Stones: A Randomized Controlled Trial. Int J Clin Pract. 2022 Jan 31;2022:3757588. doi: 10.1155/2022/3757588. eCollection 2022.
Results Reference
derived
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Tamsulosin as Adjunctive Therapy After Extracorporeal Shock Wave Lithotripsy for Renal Stones
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