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CompletedNCT00007085Updated Jul 29, 2016

Prospective Investigation of Pulmonary Embolism Diagnosis (PIOPED II)

An interventional study of Tomography, X-ray Computed in Lung Diseases, Pulmonary Embolism and Venous Thromboembolism, sponsored by National Heart, Lung, and Blood Institute (NHLBI). Completed. Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2016-07-29.

Sponsored by National Heart, Lung, and Blood Institute (NHLBI) · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Ages
18 Years to 100 Years
Sex
All
01

Study summary

To determine the value of contrast enhanced spiral computed tomography (spiral CT) for the diagnosis of acute pulmonary embolism (PE).

Read the detailed description

BACKGROUND:

Approximately 600,000 Americans sustain pulmonary embolism each year; one-third of these episodes are fatal. Unfortunately, pulmonary embolism is underdiagnosed and, therefore, under-treated. A substantial body of evidence suggests that the diagnosis of pulmonary embolism is not made in the majority of patients in whom it causes or contributes to death.

In the main, there are two explanations for the failure to diagnose pulmonary embolism: pulmonary embolism may be clinically silent, and there is no definitive, noninvasive diagnostic test. Indeed, ventilation perfusion lung scans are nondiagnostic in the majority of patients with suspected acute pulmonary embolism. Pulmonary angiography may be used to establish a diagnosis in such patients, but it is underutilized because of a mortality risk around 1 percent.

Recently, relatively small studies have suggested that contrast enhanced spiral computed tomography (CT) scanning is a useful diagnostic test for pulmonary embolism, with sensitivity as high as 80 percent and specificity as high as 95 percent. Spiral CT is widely available and much less invasive than pulmonary angiography. If spiral CT could be established as a useful diagnostic test, pulmonary embolism would be diagnosed more effectively and more patients would receive proper treatment.

DESIGN NARRATIVE:

The study evaluates the role of spiral CT scan in the diagnosis of PE by comparison with a composite reference test, including pulmonary angiography, V/Q lung scan in patients without prior PE and compression ultrasound of the lower extremities in patients with no prior deep venous thrombosis (DVT).

02

Conditions studied

  • Lung Diseases
  • Pulmonary Embolism
  • Venous Thromboembolism
03

In context

Lung Diseases

3,303 studies on the registry are indexed under Lung Diseases; 355 are open to participants now.

Browse Lung Diseases studies →

Lead sponsor

National Heart, Lung, and Blood Institute (NHLBI) is the lead sponsor of 1,117 studies on the registry; 71 are open to participants now.

Of its 57 completed or terminated interventional studies of FDA-regulated products, 49 (86%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

> 18% normal kidney function, no dye allergies, suspected of acute pulmonary embolism

05

Study design

Phase
Not applicable
Primary purpose
Diagnostic

Interventions

  • DeviceTomography, X-ray Computed
06

Study locations

No study locations are listed for this record.

07

References and documents

Publications

  • Gottschalk A, Stein PD, Goodman LR, Sostman HD. Overview of Prospective Investigation of Pulmonary Embolism Diagnosis II. Semin Nucl Med. 2002 Jul;32(3):173-82. doi: 10.1053/snuc.2002.124177. PubMed 12105798 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 29, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00007085
Lead sponsor
National Heart, Lung, and Blood Institute (NHLBI)
First posted
Dec 8, 2000
Start date
Sep 2000
Primary completion
Dec 2004
Completion
Dec 2004
Last update
Jul 29, 2016

Study contacts

Sarah Fowler
George Washington University
Charles Hales
Massachusetts General Hospital
Russell Hull
University of Calgary
Kenneth Leeper
Emory University
John Popovich
Case Western Reserve Univ-Henry Ford HSC
Henry Sostman
Weill Medical College of Cornell University
Paul Stein
St. Joseph Mercy
Victor Tapson
Duke University
John Weg
University of Michigan at Ann Arbor
Pamela Woodard
Washington University School of Medicine
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2008. You cannot join it, but the record below documents what was studied.

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