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NCT04922307Active, not recruiting

Reduction of Allogenic Blood Transfusion in Locally Advanced Kidney Cancer

Source: ClinicalTrials.gov · Last updated 12 Nov 2025

Brief summary (registry, in English)

The Reduction of Allogenic Blood Transfusion in Locally Advanced Kidney Cancer Trial (RESTRICT). The primary objective is to reduce the number of units of allogenic blood transfusion in locally advanced kidney cancer (≥ cT2). Secondary objectives include reduction in perioperative complications, assessment of recurrence free-survival and improving overall survival.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
240 (estimated)
First submitted
4 Jun 2021
Start date
23 Jul 2021
Primary completion date
12 Feb 2025
Lead sponsor
Vanderbilt University Medical Center
NCT number
NCT04922307

What you commit to

  • Study type: Interventional
  • Planned participants: 240
  • From 23 Jul 2021 to the primary completion date, 12 Feb 2025
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Non-surgical candidate

Other illness

  • Unstable angina.

Age

  • Male and female younger than 18 years old.

Who the study is looking for

  • Renal masses ≥ cT2 (by any conventional imaging).
  • N1 or M1 disease is allowed if they are deemed surgical candidates (including cytoreductive nephrectomy).
  • Male and female patients.
  • 18 and older.
  • Ejection fraction (EF) ≥ 45% by echocardiogram (ECHO).
  • Adequate organ function as defined by:
    • Hemoglobin ≥ 9 g/dL. Pre-operative allogenic blood transfusion is allowed.
    • Platelets ≥ 100.000/μl.
    • Albumin ≥ 2.5 g/dL.
    • Aspartate Aminotransferase (AST) and alanine transaminase (ALT) ≤ 75U/L or total bilirubin ≤ 2.0 mg/dL.
    • WBC within institutional normal limits.
    • PT within institutional normal limits.
    • INR \< 1.5 and PTT normal.
    • Consent and compliance with all aspects of the study protocol.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Winship Cancer Institute at Emory University
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
Vanderbilt University Medical Center
Coordinator of this site? Confirm its status
NashvilleUnited StatesUnknown status
H Lee Moffitt Cancer Center
Coordinator of this site? Confirm its status
TampaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.