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Clamped or Unclamped Surgery in Treating Patients With Kidney Cancer

Primary Purpose

Recurrent Renal Cell Cancer

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
robot-assisted laparoscopic surgery
robot-assisted laparoscopic surgery
Sponsored by
University of Southern California
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Recurrent Renal Cell Cancer

Eligibility Criteria

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

Inclusion Criteria:

  • Solitary renal mass or solitary complex renal cyst Bosniak >/= Grade 3
  • Clinical stage T1a, T1b
  • Body Mass Index (BMI) < 40
  • Surgical candidate (preoperative cardiac and anesthesia clearance obtained)
  • Able to give informed consent
  • 24 hour urine collection complete and report obtained
  • MAG-3/DTPA scan completed and report obtained

Exclusion Criteria:

  • Pregnancy
  • More than 1 renal mass or complex renal cyst Bosniak >/= Grade 3 on ipsilateral kidney
  • Previous renal surgery on the ipsilateral kidney
  • Clinical Stage T2 or greater
  • BMI > 40
  • Contraindication to systemic hypotension:

    • Left Main Coronary Arterial Disease
    • Severe cardiac decompensation (ejection fraction [EF] < 40%)
    • Prior history of cerebrovascular accident
  • Unable to consent
  • Unwilling or unable to potentially receive blood transfusion

Sites / Locations

  • USC/Norris Comprehensive Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Arm A (unclamped partial nephrectomy)

Arm B (clamped partial nephrectomy)

Arm Description

Patients undergo unclamped partial nephrectomy. Some patients may undergo unclamped partial nephrectomy with controlled hypotension.

Patients undergo clamped partial nephrectomy.

Outcomes

Primary Outcome Measures

Change from baseline in renal function as measured by eGFR
Measured by eGFR, MAG-3 Nuclear Renal Scan, and serum creatinine. The two arms will be compared using regression methods that will account for repeated measures and the pre-randomization stratification.

Secondary Outcome Measures

Estimated blood loss during surgery
Rate of blood transfusion during and after surgery
Number of patients with positive surgical margins
Number of patients with complications during surgery and at 90 days post surgery
Number of patients with adverse events
Intra-renal blood flow measurements
Resistive index measurements

Full Information

First Posted
February 10, 2012
Last Updated
March 25, 2015
Sponsor
University of Southern California
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT01547676
Brief Title
Clamped or Unclamped Surgery in Treating Patients With Kidney Cancer
Official Title
Prospective Randomized Comparison of Clamped Versus Unclamped Partial Nephrectomy
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Terminated
Why Stopped
P.I. decided to terminate study due to multiple unresolved issues
Study Start Date
December 2011 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Southern California
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This randomized pilot trial studies clamped or unclamped surgery in treating patients with kidney cancer. Unclamped surgery for kidney cancer may have fewer side effects
Detailed Description
PRIMARY OBJECTIVES: I. To compare the changes in renal function (post-operative compared to pre-operative) in patients undergoing unclamped partial nephrectomy with or without controlled hypotension (Arm A) vs. those undergoing partial nephrectomy with hilar clamping (Arm B), as measured by change in estimated glomerular filtration rate (eGFR). SECONDARY OBJECTIVES: I. To compare the changes in renal function (post-operative compared to pre-operative) in patients undergoing unclamped partial nephrectomy with or without controlled hypotension (Arm A) vs. those undergoing partial nephrectomy with hilar clamping (Arm B), as measured by change in MAG3 (% of function attributed to affected kidney) and change in serum creatinine. II. To evaluate the safety of the unclamped procedure by estimating the differences in complication rates in patients undergoing unclamped partial nephrectomy with or without controlled hypotension (Arm A) vs. patients undergoing partial nephrectomy with hilar clamping (Arm B) in terms of intra-operative complications and post-operative complications. III. To evaluate the surgical effectiveness of the unclamped procedure by estimating the differences between patients undergoing unclamped partial nephrectomy with or without controlled hypotension (Arm A) vs. patients undergoing partial nephrectomy with hilar clamping (Arm B) in terms of surgical margin status, estimated blood loss, and transfusion rate (intraoperative and post-operative). TERTIARY OBJECTIVES: I. To record and compare the intrarenal blood flow and resistive index measurements in order to determine if a relationship exists between intraoperative findings and postoperative renal function. II. To quantify the amount of acute kidney injury (AKI) and compare the differences between patients undergoing unclamped partial nephrectomy with or without controlled hypotension (Arm A) vs. patients undergoing partial nephrectomy with hilar clamping (Arm B) as measured by urinary and serum biomarkers. III. To compare the effects of the unclamped procedure (Arm A) to the clamped procedure (Arm B) in patients with baseline eGFR < 60, and in patients with age >= 75 (exploratory subset analyses). OUTLINE: Patients are randomized to 1 of 2 treatment arms. ARM A: Patients undergo unclamped partial nephrectomy. Some patients may undergo unclamped partial nephrectomy with controlled hypotension. ARM B: Patients undergo clamped partial nephrectomy. After completion of study treatment, patients are followed up at 1 week and then at 1, 3, 6, and 12 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Renal Cell Cancer

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm A (unclamped partial nephrectomy)
Arm Type
Experimental
Arm Description
Patients undergo unclamped partial nephrectomy. Some patients may undergo unclamped partial nephrectomy with controlled hypotension.
Arm Title
Arm B (clamped partial nephrectomy)
Arm Type
Active Comparator
Arm Description
Patients undergo clamped partial nephrectomy.
Intervention Type
Procedure
Intervention Name(s)
robot-assisted laparoscopic surgery
Intervention Description
Unclamped partial nephrectomy
Intervention Type
Procedure
Intervention Name(s)
robot-assisted laparoscopic surgery
Intervention Description
Undergo clamped partial nephrectomy
Primary Outcome Measure Information:
Title
Change from baseline in renal function as measured by eGFR
Description
Measured by eGFR, MAG-3 Nuclear Renal Scan, and serum creatinine. The two arms will be compared using regression methods that will account for repeated measures and the pre-randomization stratification.
Time Frame
Up to 1 year
Secondary Outcome Measure Information:
Title
Estimated blood loss during surgery
Time Frame
Up to 1 year
Title
Rate of blood transfusion during and after surgery
Time Frame
Up to 1 year
Title
Number of patients with positive surgical margins
Time Frame
Up to 1 year
Title
Number of patients with complications during surgery and at 90 days post surgery
Time Frame
Up to 1 year
Title
Number of patients with adverse events
Time Frame
Up to 1 year
Title
Intra-renal blood flow measurements
Time Frame
Up to 1 year
Title
Resistive index measurements
Time Frame
Up to 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Solitary renal mass or solitary complex renal cyst Bosniak >/= Grade 3 Clinical stage T1a, T1b Body Mass Index (BMI) < 40 Surgical candidate (preoperative cardiac and anesthesia clearance obtained) Able to give informed consent 24 hour urine collection complete and report obtained MAG-3/DTPA scan completed and report obtained Exclusion Criteria: Pregnancy More than 1 renal mass or complex renal cyst Bosniak >/= Grade 3 on ipsilateral kidney Previous renal surgery on the ipsilateral kidney Clinical Stage T2 or greater BMI > 40 Contraindication to systemic hypotension: Left Main Coronary Arterial Disease Severe cardiac decompensation (ejection fraction [EF] < 40%) Prior history of cerebrovascular accident Unable to consent Unwilling or unable to potentially receive blood transfusion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mihir Desai
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
Facility Information:
Facility Name
USC/Norris Comprehensive Cancer Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States

12. IPD Sharing Statement

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Clamped or Unclamped Surgery in Treating Patients With Kidney Cancer

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