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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
Hospital Regional de Alta Especialidad del Bajio
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Stone focused on measuring Extracorporeal shock wave lithotripsy, Tamsulosin, Urolithiasis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    March 25, 2021
    Last Updated
    March 26, 2021
    Sponsor
    Hospital Regional de Alta Especialidad del Bajio
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    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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