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NCT00607828 · ClinicalTrials.gov registry record · NA

Stereotactic Radiation Therapy in Treating Patients With Advanced Liver Cancer

A NA study, sponsored by University of Nebraska.

Completed
Registry status
NA
Development phase
7
Enrollment target

NCT00607828: Completed NA study, sponsored by University of Nebraska.

NCT00607828 is a NA study that has completed, run by University of Nebraska. The registered enrollment target is 7 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

NCT00607828, a NA study, has completed, sponsored by University of Nebraska.

COMPLETED
Registry status
NA
Development phase
7 participants
Enrollment target

Study Summary

This is a phase I trial studying the side effects and best dose of stereotactic radiation therapy (SRT) in treating patients with advanced liver cancer. Stereotactic radiation therapy may be able to send x-rays directly to the tumor and cause less damage to normal tissue.

Primary Outcome

Toxicity as assessed by NCI CTCAE v3.0 (Adverse Events). Due to delayed toxicities attributable to radiotherapy, all toxicities observed within 1 month after SRT will be scored. Dose limiting toxicity (DLT) is defined as any of following toxicities, that is possibly, probably or definitely related to Stereotactic Radiation Therapy (SRT) occurring within 1 month from the start of treatment: 1. grade 4 or 5 hepatic 2. grade 4 or 5 gastrointestinal 3. grade 4 or 5 thrombocytopenia 4. grade 4 hepat

Interventions

  • RADIATION stereotactic body radiation therapy

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2007-11-16
Est. Completion 2017-02-15
Phase NA
University of Nebraska

407 total trials

What the finished NCT00607828 record still lists

NCT00607828 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 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 1 intervention - of which stereotactic body radiation therapy is the first listed.

NCT00607828 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00607828 about?

NCT00607828 is a clinical study titled "Stereotactic Radiation Therapy in Treating Patients With Advanced Liver Cancer". This is a phase I trial studying the side effects and best dose of stereotactic radiation therapy (SRT) in treating patients with advanced liver cancer. Stereotactic radiation therapy may be able to send x-rays directly to the tumor and cause less damage to normal tissue.

What is the current status of trial NCT00607828?

This trial is currently completed. It is a NA study. The enrollment target is 7 participants. The study started on 2007-11-16. Estimated completion is 2017-02-15.

What interventions are being tested in trial NCT00607828?

The interventions under investigation include: stereotactic body radiation therapy (RADIATION).

Who is sponsoring clinical trial NCT00607828?

This trial is sponsored by University of Nebraska, which has 407 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00607828's enrollment target sits among peer trials

7 1982nd of 2000 higher than 18 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 NCT00607828, the US trial registry maintained by the National Library of Medicine. NCT00607828 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.