← Back to Search

VQ vs. CT Scans for Preventing Acute Kidney Injury (VQ/CT Trial)

N/A
Recruiting
Research Sponsored by Indiana University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age≥18 years
CTPA ordered by the treating provider to evaluate PE
Timeline
Screening 3 weeks
Treatment Varies
Follow Up >/= 48 hours to </= 168 hours of enrollment
Awards & highlights

VQ/CT Trial Summary

This trial is studying whether using a VQ scan instead of a CT scan to look for pulmonary embolism can help prevent kidney problems in patients.

Who is the study for?
This trial is for adults who might have a pulmonary embolism but are at low risk (≤20% chance) and have a moderate to high risk of developing kidney problems from IV dye (CINRisk Score ≥2). It's not for those with recent or upcoming contrast exposure, history of certain lung conditions, pregnancy, active dialysis, renal transplant, or clinical instability.Check my eligibility
What is being tested?
The study compares two imaging tests: CT scans that use IV dye and V/Q scans that don't. The goal is to see if the V/Q scan can prevent contrast-induced kidney damage in patients needing evaluation for possible pulmonary embolism.See study design
What are the potential side effects?
CT scan side effects may include allergic reactions to the dye leading to kidney issues known as CIN which often has no symptoms but requires blood tests. V/Q scans generally do not involve these risks as they use different substances.

VQ/CT Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am 18 years old or older.
Select...
My doctor has ordered a CT scan to check for blood clots in my lungs.

VQ/CT Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~>/= 48 hours to </= 168 hours of enrollment
This trial's timeline: 3 weeks for screening, Varies for treatment, and >/= 48 hours to </= 168 hours of enrollment for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Acute kidney injury in subjects exposed and unexposed to iodinated contrast media
Secondary outcome measures
Validate the acute kidney injury score, alone and in combination with acute-phase markers of renal dysfunction.

VQ/CT Trial Design

3Treatment groups
Active Control
Group I: Randomized to V/QActive Control1 Intervention
300 patients with > 25% estimated risk of CIN (CINRisk Score ≥ 2), randomized to VQ imaging (unexposed control)
Group II: Low risk for kidney injury with use of CTActive Control1 Intervention
No randomization due to low risk for kidney injury. 100 patients undergoing CTPA with an estimated risk of CIN <10% (CINRisk Score <2)
Group III: Randomized to CTActive Control1 Intervention
300 patients with > 25% estimated risk of CIN (CINRisk Score ≥ 2), randomized to CT (exposure to iodinated contrast media)

Find a Location

Who is running the clinical trial?

National Heart, Lung, and Blood Institute (NHLBI)NIH
3,837 Previous Clinical Trials
47,850,927 Total Patients Enrolled
19 Trials studying Pulmonary Embolism
149,055 Patients Enrolled for Pulmonary Embolism
Indiana UniversityLead Sponsor
980 Previous Clinical Trials
982,576 Total Patients Enrolled

Media Library

Computed tomography scan Clinical Trial Eligibility Overview. Trial Name: NCT03116139 — N/A
Pulmonary Embolism Research Study Groups: Randomized to V/Q, Low risk for kidney injury with use of CT, Randomized to CT
Pulmonary Embolism Clinical Trial 2023: Computed tomography scan Highlights & Side Effects. Trial Name: NCT03116139 — N/A
Computed tomography scan 2023 Treatment Timeline for Medical Study. Trial Name: NCT03116139 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~63 spots leftby Dec 2024