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NCT01613521 · ClinicalTrials.gov registry record · NA

Tumor Perfusion and Hypoxia Assessed by DCE-MRI and 18F-FMISO PET as Biomarkers of Treatment Response in Cervical Cancer

A NA study, sponsored by Memorial Sloan Kettering Cancer Center.

Terminated
Registry status
NA
Development phase
3
Enrollment target

NCT01613521: Clinical Trial NA study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT01613521 is a NA study that was terminated before completion, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 3 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01613521, a NA study, was terminated before completion, sponsored by Memorial Sloan Kettering Cancer Center.

TERMINATED
Registry status
NA
Development phase
3 participants
Enrollment target

Study Summary

This study is to assess how patients respond to their treatment for cervical cancer. This research does not involve a specific treatment for the cancer that will be recommended by the doctor and may include radiation therapy and/or chemotherapy. This is a separate research imaging study designed to assess how patients respond to their treatment for cervical cancer.

Interventions

  • OTHER DCE-MRI and 18F-FMISO PET

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2012-06
Est. Completion 2014-03
Phase NA

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT01613521

The ClinicalTrials.gov registry entry for NCT01613521 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 3 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which DCE-MRI and 18F-FMISO PET is the first listed.

NCT01613521 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01613521 about?

NCT01613521 is a clinical study titled "Tumor Perfusion and Hypoxia Assessed by DCE-MRI and 18F-FMISO PET as Biomarkers of Treatment Response in Cervical Cancer". This study is to assess how patients respond to their treatment for cervical cancer. This research does not involve a specific treatment for the cancer that will be recommended by the doctor and may include radiation therapy and/or chemotherapy. This is a separate research imaging study designed to ...

What is the current status of trial NCT01613521?

This trial is currently terminated. It is a NA study. The enrollment target is 3 participants. The study started on 2012-06. Estimated completion is 2014-03.

What interventions are being tested in trial NCT01613521?

The interventions under investigation include: DCE-MRI and 18F-FMISO PET (OTHER).

Who is sponsoring clinical trial NCT01613521?

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

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.