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NCT01424956 · ClinicalTrials.gov registry record
CRRS-4 Pivotal Somo•v™ ABUS ROC Reader Observer Study
A clinical trial of Breast Cancer, sponsored by U-Systems.
- Completed
- Registry status
- 17
- Enrollment target
- 1
- Study location
NCT01424956: Completed study of Breast Cancer, sponsored by U-Systems.
NCT01424956 is a study of Breast Cancer that has completed, run by U-Systems. The registered enrollment target is 17 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01424956, a study of Breast Cancer, has completed, sponsored by U-Systems.
- COMPLETED
- Registry status
- 17 participants
- Enrollment target
- 1
- Study location
Study Summary
To determine the impact on Interpreting Physician performance in detecting breast cancer, as defined by the area under the Receiver Operating Characteristic Curve (ROC), when Automated Breast Ultrasound (ABUS) and screening mammography (XRM) are combined, compared to screening mammography alone in asymptomatic women with \>50% parenchymal density and a screening mammogram assigned a BI-RADS Assessment Category 1 (negative) or 2 (normal with benign findings). The effect of the improved Reader performance is illustrated by plotting the ROC curves for XRM alone and XRM+ABUS. If Reader performance improves with the addition of ABUS to the XRM, the area under the curve (AUC) for XRM+ABUS (AUCXRM+ABUS) will be greater than the area under the curve for XRM Alone (AUCXRM Alone). This difference is represented as ∆AUCABUS. The null and alternative hypotheses can be formally expressed as follows: H0: ∆AUCABUS = 0, AUCXRM+ABUS = AUCXRM Alone The null hypothesis is that Reader performance will be unchanged with the addition of ABUS to a screening mammogram assigned a BI-RADS Assessment Category of 1 or 2. HA: ∆AUCABUS ≠ 0, AUCXRM+ABUS ≠ AUCXRM Alone The alternative hypothesis is that Reader performance will be changed with the addition of ABUS to a screening mammogram assigned a BI-RADS Assessment Category of 1 or 2. A statistically significant change will be considered equivalent to a statistically significant improvement if the estimated value of AUCXRM+ABUS is greater than that of AUCXRM Alone with statistical significance at an alpha level of .05 for a two-sided test.
Primary Outcome
To determine the impact on Interpreting Physician (Reader) Performance in detecting breast cancer, as defined by the area under the Receiver Operating Characteristic (ROC) Curve (AUC), when ABUS and XRM are combined (XRM+ABUS), compared to XRM Alone in asymptomatic women with \>50% parenchymal density (BI-RADS Composition/Density rating of 3 or 4) and a screening mammogram assigned a BI-RADS Assessment Category 1 (negative) or 2 (normal with benign findings).
Conditions Studied
Interventions
- DEVICE Automated Breast Ultrasound (ABUS)
Study Locations (1)
California
- U-Systems, Inc. - Sunnyvale
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 17 participants |
| Start Date | 2011-07 |
| Est. Completion | 2011-09 |
What the finished NCT01424956 record still lists
NCT01424956 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (99% lower).
The record links to 1 condition, with Breast Cancer appearing as the primary indexed condition, and to 1 intervention - of which Automated Breast Ultrasound (ABUS) is the first listed.
NCT01424956 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT01424956 about?
NCT01424956 is a clinical study titled "CRRS-4 Pivotal Somo•v™ ABUS ROC Reader Observer Study". To determine the impact on Interpreting Physician performance in detecting breast cancer, as defined by the area under the Receiver Operating Characteristic Curve (ROC), when Automated Breast Ultrasound (ABUS) and screening mammography (XRM) are combined, compared to screening mammography alone in a...
What is the current status of trial NCT01424956?
This trial is currently completed. The enrollment target is 17 participants. The study started on 2011-07. Estimated completion is 2011-09.
What conditions does trial NCT01424956 study?
This clinical trial studies the following conditions: Breast Cancer.
What interventions are being tested in trial NCT01424956?
The interventions under investigation include: Automated Breast Ultrasound (ABUS) (DEVICE).
Who is sponsoring clinical trial NCT01424956?
This trial is sponsored by U-Systems, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01424956 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT01424956's enrollment target sits among peer trials
17 1129th of 1224 higher than 91 of 1,224 other Breast Cancer trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Breast Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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