Ongoing registered clinical trials assessing the effect of endourological procedures on renal injury using biomarkers
NCT number . | Study design . | Study population . | Endourological technique . | Biomarker . | Time points of renal function assessment . | Status and estimated completion date . |
---|---|---|---|---|---|---|
NCT02522689 | Two parallel-arms, open- label randomized clinical study | 60 participants (30 per group) with renal stone <2 cm | Ultra-mini PCNL versus micro-PCNL | Cystatin C (blood, urine) | Preoperative versus 12 h post-operative |
|
NCT02522676 | Six parallel-arms, open-label randomized clinical study | 300 (50 per group) participants with lower pole and/or renal pelvis stone(s) | PCNL versus mini-PCNL versus ultramini-PCNL versus micro-PCNL versus RIRS versus ESWL |
| Preoperative versus 6-, 12-, 24-, 48- and 72-h post-operative |
|
NCT03112499 | Three parallel-arms, open-label randomized clinical study | 75 (25 per group) participants with renal stone 1–3 cm | PCNL versus mini-PCNL versus RIRS |
| 2-h preoperative and 2, 6, 24 and 48 h post-operative |
|
NCT number . | Study design . | Study population . | Endourological technique . | Biomarker . | Time points of renal function assessment . | Status and estimated completion date . |
---|---|---|---|---|---|---|
NCT02522689 | Two parallel-arms, open- label randomized clinical study | 60 participants (30 per group) with renal stone <2 cm | Ultra-mini PCNL versus micro-PCNL | Cystatin C (blood, urine) | Preoperative versus 12 h post-operative |
|
NCT02522676 | Six parallel-arms, open-label randomized clinical study | 300 (50 per group) participants with lower pole and/or renal pelvis stone(s) | PCNL versus mini-PCNL versus ultramini-PCNL versus micro-PCNL versus RIRS versus ESWL |
| Preoperative versus 6-, 12-, 24-, 48- and 72-h post-operative |
|
NCT03112499 | Three parallel-arms, open-label randomized clinical study | 75 (25 per group) participants with renal stone 1–3 cm | PCNL versus mini-PCNL versus RIRS |
| 2-h preoperative and 2, 6, 24 and 48 h post-operative |
|
Ongoing registered clinical trials assessing the effect of endourological procedures on renal injury using biomarkers
NCT number . | Study design . | Study population . | Endourological technique . | Biomarker . | Time points of renal function assessment . | Status and estimated completion date . |
---|---|---|---|---|---|---|
NCT02522689 | Two parallel-arms, open- label randomized clinical study | 60 participants (30 per group) with renal stone <2 cm | Ultra-mini PCNL versus micro-PCNL | Cystatin C (blood, urine) | Preoperative versus 12 h post-operative |
|
NCT02522676 | Six parallel-arms, open-label randomized clinical study | 300 (50 per group) participants with lower pole and/or renal pelvis stone(s) | PCNL versus mini-PCNL versus ultramini-PCNL versus micro-PCNL versus RIRS versus ESWL |
| Preoperative versus 6-, 12-, 24-, 48- and 72-h post-operative |
|
NCT03112499 | Three parallel-arms, open-label randomized clinical study | 75 (25 per group) participants with renal stone 1–3 cm | PCNL versus mini-PCNL versus RIRS |
| 2-h preoperative and 2, 6, 24 and 48 h post-operative |
|
NCT number . | Study design . | Study population . | Endourological technique . | Biomarker . | Time points of renal function assessment . | Status and estimated completion date . |
---|---|---|---|---|---|---|
NCT02522689 | Two parallel-arms, open- label randomized clinical study | 60 participants (30 per group) with renal stone <2 cm | Ultra-mini PCNL versus micro-PCNL | Cystatin C (blood, urine) | Preoperative versus 12 h post-operative |
|
NCT02522676 | Six parallel-arms, open-label randomized clinical study | 300 (50 per group) participants with lower pole and/or renal pelvis stone(s) | PCNL versus mini-PCNL versus ultramini-PCNL versus micro-PCNL versus RIRS versus ESWL |
| Preoperative versus 6-, 12-, 24-, 48- and 72-h post-operative |
|
NCT03112499 | Three parallel-arms, open-label randomized clinical study | 75 (25 per group) participants with renal stone 1–3 cm | PCNL versus mini-PCNL versus RIRS |
| 2-h preoperative and 2, 6, 24 and 48 h post-operative |
|
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