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NCT00346125 · ClinicalTrials.gov registry record · NA

PET CT as Predictor of Response in Preoperative Chemotherapy for Soft Tissue Sarcoma

A NA study, sponsored by Masonic Cancer Center, University of Minnesota.

Completed
Registry status
NA
Development phase
70
Enrollment target

NCT00346125: Completed NA study, sponsored by Masonic Cancer Center, University of Minnesota.

NCT00346125 is a NA study that has completed, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 70 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00346125, a NA study, has completed, sponsored by Masonic Cancer Center, University of Minnesota.

COMPLETED
Registry status
NA
Development phase
70 participants
Enrollment target

Study Summary

RATIONALE: Diagnostic procedures, such as positron emission tomography (PET) scan and computated tomography (CT) scan, may help doctors predict a patient's response to treatment and may help plan the best treatment. Drugs used in chemotherapy, such as doxorubicin and ifosfamide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. PURPOSE: This clinical trial is studying how well PET scan combined with CT scan predicts response in patients undergoing chemotherapy and surgery for soft tissue sarcoma.

Primary Outcome

Compare changes in baseline and follow-up fludeoxyglucose (FDG) positron emission tomography (PET)/CT imaging with disease-free survival by peak SUV and max SUV calculations. Changes in baseline and follow-up PET/CT, based on max SUV calculations, will be compared with disease free survival. Disease free survival will be measured in months from the time of study enrollment until the time that disease recurrence/relapse/progression is recorded.

Interventions

  • DRUG pegylated liposomal doxorubicin hydrochloride
  • PROCEDURE conventional surgery
  • DRUG ifosfamide
  • DRUG doxorubicin hydrochloride
  • BIOLOGICAL pegfilgrastim

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2006-04-10
Est. Completion 2022-07
Phase NA

What the finished NCT00346125 record still lists

NCT00346125 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 5 interventions - of which pegylated liposomal doxorubicin hydrochloride is the first listed.

NCT00346125 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00346125 about?

NCT00346125 is a clinical study titled "PET CT as Predictor of Response in Preoperative Chemotherapy for Soft Tissue Sarcoma". RATIONALE: Diagnostic procedures, such as positron emission tomography (PET) scan and computated tomography (CT) scan, may help doctors predict a patient's response to treatment and may help plan the best treatment. Drugs used in chemotherapy, such as doxorubicin and ifosfamide, work in different wa...

What is the current status of trial NCT00346125?

This trial is currently completed. It is a NA study. The enrollment target is 70 participants. The study started on 2006-04-10. Estimated completion is 2022-07.

What interventions are being tested in trial NCT00346125?

The interventions under investigation include: pegylated liposomal doxorubicin hydrochloride (DRUG), conventional surgery (PROCEDURE), ifosfamide (DRUG), doxorubicin hydrochloride (DRUG), pegfilgrastim (BIOLOGICAL).

Who is sponsoring clinical trial NCT00346125?

This trial is sponsored by Masonic Cancer Center, University of Minnesota, which has 249 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00346125's enrollment target sits among peer trials

70 1103rd of 2000 higher than 868 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 NCT00346125, the US trial registry maintained by the National Library of Medicine. NCT00346125 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.