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NCT03402607 · ClinicalTrials.gov registry record · NA

Trial Comparing PLA to HIGRT (PROVE-HCC)

A NA study, sponsored by Duke University.

Terminated
Registry status
NA
Development phase
12
Enrollment target

NCT03402607: Clinical Trial NA study, sponsored by Duke University.

NCT03402607 is a NA study that was terminated before completion, run by Duke University. The registered enrollment target is 12 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03402607, a NA study, was terminated before completion, sponsored by Duke University.

TERMINATED
Registry status
NA
Development phase
12 participants
Enrollment target

Study Summary

This phase II, randomized trial compare Quality of Life for patients with Hepatocellular Carcinoma (HCC) who are not surgical candidates or decline surgery and are treated with Percutaneous Local Ablation (PLA) or Hypofractionated Image-Guided Radiation Therapy (HIGRT).

Primary Outcome

To compare change in Quality of Life (QOL), as defined by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core-30 (EORTC C-30) post treatment in patients receiving PLA vs HIGRT. The EORTC QLQ-C30 reports a Summary Score that is calculated from the mean of 13 of the 15 QLQ-C30 scales (excluding Global Quality of Life scale and the Financial Impact scale). 28 of the items have a range of 1 (not at all) to 4 (very much) and two of them have a range of 1

Interventions

  • PROCEDURE Percutaneous Local Ablation
  • RADIATION Hypofractionated Image Guided Radiation Therapy

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2018-08-08
Est. Completion 2020-03-25
Phase NA
Duke University

1,725 total trials

Why NCT03402607 stopped before completion

NCT03402607 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Percutaneous Local Ablation is the first listed.

NCT03402607 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03402607 about?

NCT03402607 is a clinical study titled "Trial Comparing PLA to HIGRT (PROVE-HCC)". This phase II, randomized trial compare Quality of Life for patients with Hepatocellular Carcinoma (HCC) who are not surgical candidates or decline surgery and are treated with Percutaneous Local Ablation (PLA) or Hypofractionated Image-Guided Radiation Therapy (HIGRT).

What is the current status of trial NCT03402607?

This trial is currently terminated. It is a NA study. The enrollment target is 12 participants. The study started on 2018-08-08. Estimated completion is 2020-03-25.

What interventions are being tested in trial NCT03402607?

The interventions under investigation include: Percutaneous Local Ablation (PROCEDURE), Hypofractionated Image Guided Radiation Therapy (RADIATION).

Who is sponsoring clinical trial NCT03402607?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03402607's enrollment target sits among peer trials

12 1913th of 2000 higher than 74 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 NCT03402607, the US trial registry maintained by the National Library of Medicine. NCT03402607 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.