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NCT02768389 · ClinicalTrials.gov registry record · Early Phase 1

Feasibility Trial of the Modified Atkins Diet and Bevacizumab for Recurrent Glioblastoma

A Early Phase 1 study, sponsored by Case Comprehensive Cancer Center.

Completed
Registry status
Early Phase 1
Development phase
18
Enrollment target

NCT02768389: Completed Early Phase 1 study, sponsored by Case Comprehensive Cancer Center.

NCT02768389 is a Early Phase 1 study that has completed, run by Case Comprehensive Cancer Center. The registered enrollment target is 18 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (66% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02768389, a Early Phase 1 study, has completed, sponsored by Case Comprehensive Cancer Center.

COMPLETED
Registry status
Early Phase 1
Development phase
18 participants
Enrollment target

Study Summary

Patients may participate in this research study if they have glioblastoma. (a brain tumor) that has come back after being treated. Standard treatment for this cancer is a chemotherapy drug called bevacizumab. This research study involves bevacizumab in combination with a special diet called the Modified Atkins Diet (MAD). The purpose of this study is to research if patients can stay on the MAD when it is added to the standard bevacizumab treatment.

Primary Outcome

The number of patients following a Modified Atkins Diet for at least 80% of the time as a measure of feasibility

Interventions

  • DRUG Bevacizumab
  • BEHAVIORAL Modified Atkins Diet

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2016-09-06
Est. Completion 2018-11
Phase Early Phase 1
Case Comprehensive Cancer Center

407 total trials

What the finished NCT02768389 record still lists

NCT02768389 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (66% lower).

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

NCT02768389 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02768389 about?

NCT02768389 is a clinical study titled "Feasibility Trial of the Modified Atkins Diet and Bevacizumab for Recurrent Glioblastoma". Patients may participate in this research study if they have glioblastoma. (a brain tumor) that has come back after being treated. Standard treatment for this cancer is a chemotherapy drug called bevacizumab. This research study involves bevacizumab in combination with a special diet called the Modi...

What is the current status of trial NCT02768389?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 18 participants. The study started on 2016-09-06. Estimated completion is 2018-11.

What interventions are being tested in trial NCT02768389?

The interventions under investigation include: Bevacizumab (DRUG), Modified Atkins Diet (BEHAVIORAL).

Who is sponsoring clinical trial NCT02768389?

This trial is sponsored by Case Comprehensive Cancer Center, which has 407 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02768389's enrollment target sits among peer trials

18 1316th of 2000 higher than 651 of 2,000 other Early Phase 1 trials

participants (enrollment target), bucketed by value

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

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Source: ClinicalTrials.gov NCT02768389, the US trial registry maintained by the National Library of Medicine. NCT02768389 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.