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NCT01655745 · ClinicalTrials.gov registry record · NA

Positron Emission Tomography (PET) Study for Staging of Muscle Invasive Bladder Cancer

A NA study, sponsored by UNC Lineberger Comprehensive Cancer Center.

Completed
Registry status
NA
Development phase
22
Enrollment target

NCT01655745: Completed NA study, sponsored by UNC Lineberger Comprehensive Cancer Center.

NCT01655745 is a NA study that has completed, run by UNC Lineberger Comprehensive Cancer Center. The registered enrollment target is 22 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01655745, a NA study, has completed, sponsored by UNC Lineberger Comprehensive Cancer Center.

COMPLETED
Registry status
NA
Development phase
22 participants
Enrollment target

Study Summary

This prospective pilot study will enroll 30 patients with cT2/T3-N0-M0 urothelial carcinoma of the bladder for whom radical cystectomy with pelvic lymph node dissection is planned. This pilot study is designed to provide preliminary information on the accuracy of \[18F\] Fluorodeoxyglucose Positron Emission Tomography MRI (FDG-PET-MRI) in the staging of muscle-invasive bladder cancer.

Primary Outcome

The sensitivity and specificity of the FDG-PET-MRI for staging of muscle-invasive bladder will be evaluated by using the pathology from the radical cystectomy and lymph node dissection specimen or biopsy as the reference standard. The sensitivity and specificity of FDG-PET-MRI will be compared to conventional CT performed in all patients in this pilot study and FDG-PET-CT.

Interventions

  • PROCEDURE FDG PET/MR

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2012-07-24
Est. Completion 2019-02-01
Phase NA

What the finished NCT01655745 record still lists

NCT01655745 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which FDG PET/MR is the first listed.

NCT01655745 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01655745 about?

NCT01655745 is a clinical study titled "Positron Emission Tomography (PET) Study for Staging of Muscle Invasive Bladder Cancer". This prospective pilot study will enroll 30 patients with cT2/T3-N0-M0 urothelial carcinoma of the bladder for whom radical cystectomy with pelvic lymph node dissection is planned. This pilot study is designed to provide preliminary information on the accuracy of \[18F\] Fluorodeoxyglucose Positron ...

What is the current status of trial NCT01655745?

This trial is currently completed. It is a NA study. The enrollment target is 22 participants. The study started on 2012-07-24. Estimated completion is 2019-02-01.

What interventions are being tested in trial NCT01655745?

The interventions under investigation include: FDG PET/MR (PROCEDURE).

Who is sponsoring clinical trial NCT01655745?

This trial is sponsored by UNC Lineberger Comprehensive Cancer Center, which has 366 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01655745's enrollment target sits among peer trials

22 1756th of 2000 higher than 239 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

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Source: ClinicalTrials.gov NCT01655745, the US trial registry maintained by the National Library of Medicine. NCT01655745 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.