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NCT01760941 · ClinicalTrials.gov registry record · NA

Compassionate Same-Day Evaluation & Delivery of XRT for Bony Metastasis in Hospice Patients

A NA study, sponsored by Virginia Commonwealth University.

Terminated
Registry status
NA
Development phase
1
Enrollment target

NCT01760941: Clinical Trial NA study, sponsored by Virginia Commonwealth University.

NCT01760941 is a NA study that was terminated before completion, run by Virginia Commonwealth University. The registered enrollment target is 1 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01760941, a NA study, was terminated before completion, sponsored by Virginia Commonwealth University.

TERMINATED
Registry status
NA
Development phase
1 participants
Enrollment target

Study Summary

This is a survey study to evaluate the feasibility and effectiveness of an affordable, $400 flat rate, same-day consultation, simulation, and delivery of a single fraction of palliative radiation therapy for patients with symptomatic bony metastatic disease who are currently enrolled in hospice. Treatment planning and delivery of palliative radiotherapy will utilize "standard of care" techniques.

Primary Outcome

Patient evaluation will consist of surveys conducted at the time of treatment measured by the Radiation Oncologist Evaluation and Feasibility Assessments survey

Interventions

  • OTHER Quality-of-Life Assessment
  • OTHER Survey Administration
  • RADIATION Radiation Therapy

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2013-03
Est. Completion 2015-06
Phase NA
Virginia Commonwealth University

558 total trials

Why NCT01760941 stopped before completion

NCT01760941 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 1 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 3 interventions - of which Quality-of-Life Assessment is the first listed.

NCT01760941 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01760941 about?

NCT01760941 is a clinical study titled "Compassionate Same-Day Evaluation & Delivery of XRT for Bony Metastasis in Hospice Patients". This is a survey study to evaluate the feasibility and effectiveness of an affordable, $400 flat rate, same-day consultation, simulation, and delivery of a single fraction of palliative radiation therapy for patients with symptomatic bony metastatic disease who are currently enrolled in hospice. Tre...

What is the current status of trial NCT01760941?

This trial is currently terminated. It is a NA study. The enrollment target is 1 participants. The study started on 2013-03. Estimated completion is 2015-06.

What interventions are being tested in trial NCT01760941?

The interventions under investigation include: Quality-of-Life Assessment (OTHER), Survey Administration (OTHER), Radiation Therapy (RADIATION).

Who is sponsoring clinical trial NCT01760941?

This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01760941's enrollment target sits among peer trials

1 2001st of 2000 the lowest 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 NCT01760941, the US trial registry maintained by the National Library of Medicine. NCT01760941 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.