Intra-operative cone-beam computed tomography for detecting residual stones in percutaneous nephrolithotomy, a randomized controlled trial
Recruiting
- Conditions
- Kidney stonesnephrolithiasis10046708
- Registration Number
- NL-OMON54945
- Lead Sponsor
- niversitair Medisch Centrum Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 320
Inclusion Criteria
- Scheduled for percutaneous nephrolithotomy in the UMCG
- Intention to obtain a stone-free status in the upcoming procedure
- Obtained written informed consent
- Above 18 years of age
Exclusion Criteria
Pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main endpoint in this study is the stone-free status as assessed four weeks<br /><br>post-operatively by low-dose non-contrast abdominal CT. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary endpoints are the amount of PCNL procedures required per episode of 3<br /><br>months starting from the first PCNL procedure and the amount of stone-related<br /><br>events registered within a period of 12 months.</p><br>