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Investigating a Novel Modifiable Factor Affecting Renal Function After Partial Nephrectomy: Cortical Renorrhaphy

Primary Purpose

Renal Cell Carcinoma

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Non-renorrhaphy
Renorrhaphy
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Cell Carcinoma focused on measuring carcinoma, renal cell, partial nephrectomy, kidney function test, robotics

Eligibility Criteria

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

3.0 INCLUSION/EXCLUSION CRITERIA

3.1 Inclusion criteria:

  • ≥ 18 years of age.
  • Must provide written informed consent
  • Presence of cT1 renal mass by diagnostic CT assessment.
  • Scheduled for partial nephrectomy of renal mass.
  • Expected survival of at least 3 months.
  • ECOG ≤ 1.
  • Negative serum/urine pregnancy test within 24 hours for females of child bearing age prior to surgery
  • Recovered from toxicity of any prior therapy to grade 1 or better
  • If biopsy of mass has been done, pathology must be consistent with RCC.

3.2 Exclusion criteria:

  • Solitary kidney
  • Multiple or bilateral renal masses when more than one mass is operated on at the same time or within 4-months of each other.
  • Hepatic or renal toxicity (GFR <30) greater than or equal to Grade 2 (using CTCAE version 4 standard definitions)
  • Bleeding diathesis or inability to hold anticoagulation for surgery
  • Participation in another investigational trial concurrently or within 30 days
  • Significant acute or chronic medical, neurologic, or psychiatric illness in the subject that, in the judgment of the Principal Investigator, could compromise subject safety, limit the subject's ability to complete the study, and/or compromise the objectives of the study.

Sites / Locations

  • IU Health University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Cortical renorrhaphy

Non-renorrhaphy

Arm Description

Cortical renorrhaphy is performed after partial nephrectomy using a running barbed suture on MH (36mm) needle. Polymer locking clips are used to maintain tension. A base layer running stitch is performed prior to the cortical renorrhaphy.

The suture closure of the renal cortex after tumor removal is omitted. A base layer running stitch only is performed for hemostasis and urine leak prevention.

Outcomes

Primary Outcome Measures

%Loss renal volume
% loss in renal volume (cm3) of the operated kidney (post-operative CT at 4 mo vs. - pre-operative CT) using Phillips IntelliSpace portal semi-automated segmentation algorithm.

Secondary Outcome Measures

Operative and postoperative complications
Operative and postoperative complications (urine leak, bleeds) through the 4month follow-up
Resistive index
This is a "change" outcome measure. Pre and post-partial nephrectomy on the day of surgery Doppler/US arterial resistive index changes are recorded.
Surgeon survey
Postoperative surgeon survey evaluating comfort with surgery-Likert scale questionnaire
Predicted volume loss
Assess the volume loss predicted by a preoperative scoring system. The preoperative volume loss prediction will be compared to the 4month volume loss calculation based on CT scans.
%Loss in GFR
% eGFR loss from pre to postoperative (4mo) followup
Adverse events as defined by the Clavien-Dindo classification system.

Full Information

First Posted
May 1, 2014
Last Updated
November 19, 2020
Sponsor
Indiana University
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1. Study Identification

Unique Protocol Identification Number
NCT02131376
Brief Title
Investigating a Novel Modifiable Factor Affecting Renal Function After Partial Nephrectomy: Cortical Renorrhaphy
Official Title
Investigating a Novel Modifiable Factor Affecting Renal Function After Partial Nephrectomy: Cortical Renorrhaphy
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Terminated
Why Stopped
slow accrual, interim analysis showed no statistical significance
Study Start Date
May 9, 2014 (Actual)
Primary Completion Date
August 29, 2019 (Actual)
Study Completion Date
August 29, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indiana University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Preserving kidney function during removal of a kidney tumor is becoming increasingly important as rates of chronic kidney disease increase. A novel modifiable factor (suture closure of the defect caused by tumor removal) was discovered on retrospective studies to account for nearly two-thirds of the 15% volume loss commonly seen in operated kidneys. We hypothesize that a randomized controlled surgical trial will show that omitting the suture closure both preserves renal function and will not lead to unreasonable postoperative complications.
Detailed Description
Purpose: To evaluate a never before studied modifiable factor affecting renal function after partial nephrectomy: the suture closure of the renal cortex after tumor removal (renorrhaphy). Background: There is increasing interest in preserving renal function when removing renal tumors. This is partly due to studies that link chronic kidney disease with cardiovascular events and overall survival. There is an approximate loss of 10% overall renal function after partial nephrectomy along with a loss of 15% of the volume in the operated kidney. Studies point to 3 factors leading to this loss in renal function after partial nephrectomy: 1) Poor preoperative renal function, 2) Ischemia time (clamping the renal blood vessels to decrease bleeding during surgery, and 3) Loss in renal volume from the surgery. The only factor that is considered modifiable is ischemia time, especially when over 20-25-minutes in duration. Modern techniques now aid in keeping the ischemia time below the 25-minute cutoff. Leading experts from institutions such as the Cleveland Clinic, The University of Southern California, and The Mayo Clinic have concluded that the most important factor in preserving renal function, renal volume loss, is not modifiable. Specific Aims: Our question is: if we are removing non-functional tissue (tumor) then why is there a loss in renal volume (15%) and function (10%)? We hypothesize that by omitting one particular step during surgery, sewing closed the defect caused by tumor removal, we will be able to improve renal volume loss and function (RENORRHAPHY CLIP http://youtu.be/NXOtUHdigj4). Indiana University is in a unique position to study this hypothesis as two of our surgeons have routinely omitted closing the defect left after tumor removal (NO RENORRHAPHY CLIP http://youtu.be/ZisMjrm85s8). In a recently accepted abstract, we discovered that omitting the cortical closure (n=28) resulted in a 0.8% loss in glomerular filtration rate while using the closure resulted in a 7.3% loss (p=0.03). Following this discovery a 3D modeling project was performed to isolate the volume loss in operated kidneys using pre- and postoperative CT scans (not yet published). In this study, we discovered a 15% volume loss with cortical closure (n=38) compared to only a 5% loss without closure (n=20, p < 0.001). Bias and confounders cannot completely be removed from our retrospective data making it hard to believe that others will consider our hypothesis without a randomized controlled trial (RCT). We propose a RCT for robotic partial nephrectomy (20 stitch closure vs. 20 no stitch closure) with the primary outcome being volume change in the affected kidney.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Cell Carcinoma
Keywords
carcinoma, renal cell, partial nephrectomy, kidney function test, robotics

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cortical renorrhaphy
Arm Type
Active Comparator
Arm Description
Cortical renorrhaphy is performed after partial nephrectomy using a running barbed suture on MH (36mm) needle. Polymer locking clips are used to maintain tension. A base layer running stitch is performed prior to the cortical renorrhaphy.
Arm Title
Non-renorrhaphy
Arm Type
Experimental
Arm Description
The suture closure of the renal cortex after tumor removal is omitted. A base layer running stitch only is performed for hemostasis and urine leak prevention.
Intervention Type
Procedure
Intervention Name(s)
Non-renorrhaphy
Other Intervention Name(s)
renal reconstruction
Intervention Description
The suture closure of the renal cortex after tumor removal is omitted. A base layer running stitch only is performed for hemostasis and urine leak prevention.
Intervention Type
Procedure
Intervention Name(s)
Renorrhaphy
Other Intervention Name(s)
renal reconstruction
Intervention Description
After tumor resection the patient will have both a deep and cortical layer reconstruction
Primary Outcome Measure Information:
Title
%Loss renal volume
Description
% loss in renal volume (cm3) of the operated kidney (post-operative CT at 4 mo vs. - pre-operative CT) using Phillips IntelliSpace portal semi-automated segmentation algorithm.
Time Frame
4months
Secondary Outcome Measure Information:
Title
Operative and postoperative complications
Description
Operative and postoperative complications (urine leak, bleeds) through the 4month follow-up
Time Frame
through 4months
Title
Resistive index
Description
This is a "change" outcome measure. Pre and post-partial nephrectomy on the day of surgery Doppler/US arterial resistive index changes are recorded.
Time Frame
In the operating room prior to resection (baseline) and immediately after resection of tumor
Title
Surgeon survey
Description
Postoperative surgeon survey evaluating comfort with surgery-Likert scale questionnaire
Time Frame
immediately after surgery is complete
Title
Predicted volume loss
Description
Assess the volume loss predicted by a preoperative scoring system. The preoperative volume loss prediction will be compared to the 4month volume loss calculation based on CT scans.
Time Frame
4months
Title
%Loss in GFR
Description
% eGFR loss from pre to postoperative (4mo) followup
Time Frame
4months
Title
Adverse events as defined by the Clavien-Dindo classification system.
Time Frame
Through 4months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
3.0 INCLUSION/EXCLUSION CRITERIA 3.1 Inclusion criteria: ≥ 18 years of age. Must provide written informed consent Presence of cT1 renal mass by diagnostic CT assessment. Scheduled for partial nephrectomy of renal mass. Expected survival of at least 3 months. ECOG ≤ 1. Negative serum/urine pregnancy test within 24 hours for females of child bearing age prior to surgery Recovered from toxicity of any prior therapy to grade 1 or better If biopsy of mass has been done, pathology must be consistent with RCC. 3.2 Exclusion criteria: Solitary kidney Multiple or bilateral renal masses when more than one mass is operated on at the same time or within 4-months of each other. Hepatic or renal toxicity (GFR <30) greater than or equal to Grade 2 (using CTCAE version 4 standard definitions) Bleeding diathesis or inability to hold anticoagulation for surgery Participation in another investigational trial concurrently or within 30 days Significant acute or chronic medical, neurologic, or psychiatric illness in the subject that, in the judgment of the Principal Investigator, could compromise subject safety, limit the subject's ability to complete the study, and/or compromise the objectives of the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chandru P Sundaram, MD
Organizational Affiliation
Indiana University Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Clinton D Bahler, MD
Organizational Affiliation
Indiana University Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
IU Health University Hospital
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States

12. IPD Sharing Statement

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Investigating a Novel Modifiable Factor Affecting Renal Function After Partial Nephrectomy: Cortical Renorrhaphy

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