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NCT01109953 · ClinicalTrials.gov registry record

Improving Clinical PET/CT Image Quality in Retrospectively Reconstructed Breath-Hold Images

A clinical trial, sponsored by Memorial Sloan Kettering Cancer Center.

Terminated
Registry status
6
Enrollment target

NCT01109953: Clinical Trial study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT01109953 is a clinical trial that was terminated before completion, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 6 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01109953 was terminated before completion, sponsored by Memorial Sloan Kettering Cancer Center.

TERMINATED
Registry status
6 participants
Enrollment target

Study Summary

The patient has been referred for an FDG PET/CT scan. FDG is a form of sugar that contains a small amount of radioactivity; it is used to see the size and possible spread of cancer in the body. Pictures of the body are taken on a machine called a PET/CT scanner. The purpose of this current study is to see if we, the investigators, can take clearer pictures of the tumor than we could with our routine scan method. This would allow us to better see how FDG is picked up by the tumor. PET/CT is presently one of the best tools for detecting cancer and determining its spread in the body. However, due to breathing motion, PET and CT images may become blurred and the location of the tumor on CT and PET images may not match. We have developed a new method that enables us to reduce image blurring and to measure the tumor more accurately on PET images. In this study we want to compare two kinds of images: those from the standard PET/CT scan, and the PET/CT scan pictures taken with our new method. If successful, we may use this new method for clinical routine in the future.

Primary Outcome

Because PET events not satisfying the breathing amplitude selection criteria will be dropped off the final image set, it will be necessary to increase the acquisition time for the FOV's covering the thorax area from 3 min/bed to 5 min/bed to compensate for the reduction in statistics. This should result in a total increase of \~6 min for the whole body scan.

Interventions

  • OTHER Breath-Hold PET/CT image set

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2010-04
Est. Completion 2012-03
Memorial Sloan Kettering Cancer Center

1,884 total trials

Why NCT01109953 stopped before completion

NCT01109953 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 6 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Breath-Hold PET/CT image set is the first listed.

NCT01109953 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01109953 about?

NCT01109953 is a clinical study titled "Improving Clinical PET/CT Image Quality in Retrospectively Reconstructed Breath-Hold Images". The patient has been referred for an FDG PET/CT scan. FDG is a form of sugar that contains a small amount of radioactivity; it is used to see the size and possible spread of cancer in the body. Pictures of the body are taken on a machine called a PET/CT scanner. The purpose of this current study is...

What is the current status of trial NCT01109953?

This trial is currently terminated. The enrollment target is 6 participants. The study started on 2010-04. Estimated completion is 2012-03.

What interventions are being tested in trial NCT01109953?

The interventions under investigation include: Breath-Hold PET/CT image set (OTHER).

Who is sponsoring clinical trial NCT01109953?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01109953, the US trial registry maintained by the National Library of Medicine. NCT01109953 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.