Renal Cell Carcinoma Clinical Trial
Official title:
Investigating a Novel Modifiable Factor Affecting Renal Function After Partial Nephrectomy: Cortical Renorrhaphy
NCT number | NCT02131376 |
Other study ID # | IUCRO-0459 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | May 9, 2014 |
Est. completion date | August 29, 2019 |
Verified date | November 2020 |
Source | Indiana University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Terminated |
Enrollment | 26 |
Est. completion date | August 29, 2019 |
Est. primary completion date | August 29, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
United States | IU Health University Hospital | Indianapolis | Indiana |
Lead Sponsor | Collaborator |
---|---|
Indiana University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | %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. | 4months | |
Secondary | Operative and postoperative complications | Operative and postoperative complications (urine leak, bleeds) through the 4month follow-up | through 4months | |
Secondary | 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. | In the operating room prior to resection (baseline) and immediately after resection of tumor | |
Secondary | Surgeon survey | Postoperative surgeon survey evaluating comfort with surgery-Likert scale questionnaire | immediately after surgery is complete | |
Secondary | 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. | 4months | |
Secondary | %Loss in GFR | % eGFR loss from pre to postoperative (4mo) followup | 4months | |
Secondary | Adverse events as defined by the Clavien-Dindo classification system. | Through 4months |
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