Type of Study:

Interventional

Study Design:

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Outcome Measure:

To perfect the Renal Hypoperfusion during partial nephrectomy is feasible safe and result in better renal function than complete occlusion of renal blood flow

Outcome Description:

renal function will be measured using creatinine, eGFR, 24 hr creat clearance, and NGAL biomarker of acute kidney injury

Outcome Time Frame:

up to 2 weeks prior to surgery and up to 24 hrs post surgery

Safety Issue:

Yes

Principal Investigator

Michael Jewett, M.D.

Investigator Role:

Principal Investigator

Investigator Affiliation:

University Health Network, Toronto

Authority:

Canada: Ethics Review Committee

Study ID:

Hypoperfusion

NCT ID:

NCT01720693

Start Date:

June 2012

Completion Date:

December 2013

Related Keywords:

• Partial Nephrectomy
• Renal Cell Carcinoma
• partial nephrectomy
• hypoperfusion
• renal function
• Carcinoma
• Carcinoma, Renal Cell