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NCT00673179 · ClinicalTrials.gov registry record · NA

Doxorubicin With Cisplatin, High-Dose Methotrexate, and Additional Risk-Adapted Outpatient Chemotherapy

A NA study, sponsored by M.D. Anderson Cancer Center.

Terminated
Registry status
NA
Development phase
7
Enrollment target

NCT00673179: Clinical Trial NA study, sponsored by M.D. Anderson Cancer Center.

NCT00673179 is a NA study that was terminated before completion, run by M.D. Anderson Cancer Center. 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

NCT00673179, a NA study, was terminated before completion, sponsored by M.D. Anderson Cancer Center.

TERMINATED
Registry status
NA
Development phase
7 participants
Enrollment target

Study Summary

The goal of this clinical research study is to learn if giving certain combinations of chemotherapy drugs before and after surgery, mostly in the outpatient clinic instead of in the hospital, can result in fewer hospital stays during treatment for osteosarcoma. The drugs and schedules will vary depending on the status of the cancer and its level of risk for spreading, but they will include combinations of doxorubicin (non-liposomal), cisplatin, methotrexate, and ifosfamide, as described below.

Primary Outcome

Treatment success defined as a patient having 6 or fewer hospitalizations during front-line chemotherapy.

Interventions

  • DRUG Cisplatin
  • DRUG Doxorubicin
  • DRUG Leucovorin
  • DRUG Methotrexate
  • DRUG Dexrazoxane

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2008-05
Est. Completion 2010-11
Phase NA
M.D. Anderson Cancer Center

2,692 total trials

Why NCT00673179 stopped before completion

NCT00673179 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 5 interventions - of which Cisplatin is the first listed.

NCT00673179 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00673179 about?

NCT00673179 is a clinical study titled "Doxorubicin With Cisplatin, High-Dose Methotrexate, and Additional Risk-Adapted Outpatient Chemotherapy". The goal of this clinical research study is to learn if giving certain combinations of chemotherapy drugs before and after surgery, mostly in the outpatient clinic instead of in the hospital, can result in fewer hospital stays during treatment for osteosarcoma. The drugs and schedules will vary depe...

What is the current status of trial NCT00673179?

This trial is currently terminated. It is a NA study. The enrollment target is 7 participants. The study started on 2008-05. Estimated completion is 2010-11.

What interventions are being tested in trial NCT00673179?

The interventions under investigation include: Cisplatin (DRUG), Doxorubicin (DRUG), Leucovorin (DRUG), Methotrexate (DRUG), Dexrazoxane (DRUG).

Who is sponsoring clinical trial NCT00673179?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00673179'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 NCT00673179, the US trial registry maintained by the National Library of Medicine. NCT00673179 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.