Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01494012 · ClinicalTrials.gov registry record · Phase 1

Phase I Stereotactic Body Radiation for Metastatic or Recurrent Platinum-Resistant Ovarian Cancer

A Phase 1 study, sponsored by Stanford University.

Terminated
Registry status
Phase 1
Development phase
1
Enrollment target

NCT01494012: Clinical Trial Phase 1 study, sponsored by Stanford University.

NCT01494012 is a Phase 1 study that was terminated before completion, run by Stanford University. The registered enrollment target is 1 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT01494012, a Phase 1 study, was terminated before completion, sponsored by Stanford University.

TERMINATED
Registry status
Phase 1
Development phase
1 participants
Enrollment target

Study Summary

This phase I trial studies the side effects and the best dose of stereotactic body radiation therapy (SBRT) in treating patients with metastatic or recurrent ovarian cancer or primary peritoneal cancer. SBRT may be able to send x-rays directly to the tumor and cause less damage to normal tissue.

Primary Outcome

FDG-PET response based on interpretation by nuclear medicine physician with measurement of the maximal standard uptake value (SUV) and identification of new sites of disease. Percentage of decreased SUVmax between the pre- and post-treatment FDG-PET/CT, evaluating means, medians, range and standard deviations.

Interventions

  • OTHER questionnaire administration
  • RADIATION stereotactic body radiation therapy
  • PROCEDURE positron emission tomography
  • PROCEDURE computed tomography
  • DRUG fludeoxyglucose F 18

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2012-04
Est. Completion 2012-09
Phase Phase 1
Stanford University

1,744 total trials

Why NCT01494012 stopped before completion

NCT01494012 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 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 5 interventions - of which questionnaire administration is the first listed.

NCT01494012 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01494012 about?

NCT01494012 is a clinical study titled "Phase I Stereotactic Body Radiation for Metastatic or Recurrent Platinum-Resistant Ovarian Cancer". This phase I trial studies the side effects and the best dose of stereotactic body radiation therapy (SBRT) in treating patients with metastatic or recurrent ovarian cancer or primary peritoneal cancer. SBRT 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 NCT01494012?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 1 participants. The study started on 2012-04. Estimated completion is 2012-09.

What interventions are being tested in trial NCT01494012?

The interventions under investigation include: questionnaire administration (OTHER), stereotactic body radiation therapy (RADIATION), positron emission tomography (PROCEDURE), computed tomography (PROCEDURE), fludeoxyglucose F 18 (DRUG).

Who is sponsoring clinical trial NCT01494012?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01494012's enrollment target sits among peer trials

1 2001st of 2000 the lowest of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01494012, the US trial registry maintained by the National Library of Medicine. NCT01494012 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.