Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00707213 · ClinicalTrials.gov registry record · Phase 1

FDG-Positron Emission Tomography (PET)/CT In the Evaluation of Persistent Febrile Neutropenia in Cancer Patients

A Phase 1 study, sponsored by University of Utah.

Terminated
Registry status
Phase 1
Development phase
19
Enrollment target

NCT00707213: Clinical Trial Phase 1 study, sponsored by University of Utah.

NCT00707213 is a Phase 1 study that was terminated before completion, run by University of Utah. The registered enrollment target is 19 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00707213, a Phase 1 study, was terminated before completion, sponsored by University of Utah.

TERMINATED
Registry status
Phase 1
Development phase
19 participants
Enrollment target

Study Summary

Patients must be currently treated at the Huntsman Cancer Institute or Intermountain Primary Children's Medical Center to be eligible for this study. Although there have been many advances in the assessment and treatment of infections responsible for febrile neutropenia in cancer patients, it still remains a common complication of cancer therapy and accounts for the majority of chemotherapy-associated deaths. This National Cancer Institute (NCI) funded proposal using the R-21 Quick-Trials Exploratory Grant mechanism is to conduct an exploratory/pilot project in a group of patients with persistent febrile neutropenia to provide critical information that will support the concept, and aid in the design, of a larger multi-center clinical trial. The ultimate goal of our interdisciplinary team of oncologists, infectious diseases experts, imagers, and biostatisticians is to conduct a prospective, multi-center trial to establish the utility and cost-effectiveness of PET/CT using the widely available glucose analogue \[18F\]fluoro-2-deoxy-D-glucose (FDG) in identifying sites of infection in cancer patients with persistent febrile neutropenia without an obvious identifiable source thus improving targeted therapy.

Interventions

  • DRUG [18F]fluoro-2-deoxy-D-glucose (FDG)

Trial Details

FieldValue
Enrollment Target 19 participants
Start Date 2007-08-21
Est. Completion 2010-08-11
Phase Phase 1
University of Utah

818 total trials

Why NCT00707213 stopped before completion

NCT00707213 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 19 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (68% lower).

The record links to 0 conditions, and to 1 intervention - of which [18F]fluoro-2-deoxy-D-glucose (FDG) is the first listed.

NCT00707213 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00707213 about?

NCT00707213 is a clinical study titled "FDG-Positron Emission Tomography (PET)/CT In the Evaluation of Persistent Febrile Neutropenia in Cancer Patients". Patients must be currently treated at the Huntsman Cancer Institute or Intermountain Primary Children's Medical Center to be eligible for this study. Although there have been many advances in the assessment and treatment of infections responsible for febrile neutropenia in cancer patients, it still...

What is the current status of trial NCT00707213?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 19 participants. The study started on 2007-08-21. Estimated completion is 2010-08-11.

What interventions are being tested in trial NCT00707213?

The interventions under investigation include: [18F]fluoro-2-deoxy-D-glucose (FDG) (DRUG).

Who is sponsoring clinical trial NCT00707213?

This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00707213's enrollment target sits among peer trials

19 1716th of 2000 higher than 281 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03207464 · 19 participants · Phase 1

    Molecular Imaging of NET Using [C-11]MRB-PET in MS

  • NCT04318717 · 19 participants · Phase 2

    Pembrolizumab and Hypofractionated Radiation Therapy for the Treatment of Mucosal Melanoma

  • NCT05103904 · 19 participants · Phase 2

    Lenvatinib for the Treatment of Recurrent Hepatocellular Carcinoma After Liver Transplant

  • NCT05607407 · 19 participants · Phase 2

    Methimazole in Patients With Progressive Glioblastoma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT00707213, the US trial registry maintained by the National Library of Medicine. NCT00707213 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.