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NCT01996046 · ClinicalTrials.gov registry record

FDG PET/CT in Breast Cancer Bone Mets

A clinical trial of Estrogen Receptor-positive Breast Cancer and Bone Metastases, sponsored by University of Pennsylvania.

Active
Registry status
75
Enrollment target
1
Study location

NCT01996046 is a study of Estrogen Receptor-positive Breast Cancer and Bone Metastases that is active but no longer recruiting, run by University of Pennsylvania. The registered enrollment target is 75 participants, below the 255-participant average among 16 other Estrogen Receptor-positive Breast Cancer trials with a reported enrollment target (71% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01996046, a study of Estrogen Receptor-positive Breast Cancer and Bone Metastases, is active but no longer recruiting, sponsored by University of Pennsylvania.

ACTIVE NOT RECRUITING
Registry status
75 participants
Enrollment target
1
Study location

Study Summary

This study will evaluate baseline uptake on a FDG PET/CT scan in patients with breast cancer that has spread to the bones. A repeat FDG PET/CT scan will be done 4 weeks after the start of new breast cancer hormone treatment and again at 12 weeks after treatment start. The baseline uptake and change in uptake after the repeat scans will be compared to clinical long term outcomes such as time to progression and overall survival. In addition the uptake will be compared to the incidence of skeletal related events that are common occurrences in patients with cancer that has spread to the bones.

Interventions

  • OTHER FDG PET/CT scan

Study Locations (1)

Pennsylvania

  • University of Pennsylvania Hospital - Philadelphia

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2013-09
Est. Completion 2026-07-31

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT01996046

The ClinicalTrials.gov registry entry for NCT01996046 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 255-participant average among 16 other Estrogen Receptor-positive Breast Cancer trials with a reported enrollment target (71% lower). The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Estrogen Receptor-positive Breast Cancer appearing as the primary indexed condition, and to 1 intervention - of which FDG PET/CT scan is the first listed.

NCT01996046 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT01996046 about?

NCT01996046 is a clinical study titled "FDG PET/CT in Breast Cancer Bone Mets". This study will evaluate baseline uptake on a FDG PET/CT scan in patients with breast cancer that has spread to the bones. A repeat FDG PET/CT scan will be done 4 weeks after the start of new breast cancer hormone treatment and again at 12 weeks after treatment start. The baseline uptake and change ...

What is the current status of trial NCT01996046?

This trial is currently active not recruiting. The enrollment target is 75 participants. The study started on 2013-09. Estimated completion is 2026-07-31.

What conditions does trial NCT01996046 study?

This clinical trial studies the following conditions: Estrogen Receptor-positive Breast Cancer, Bone Metastases.

What interventions are being tested in trial NCT01996046?

The interventions under investigation include: FDG PET/CT scan (OTHER).

Who is sponsoring clinical trial NCT01996046?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01996046 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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