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NCT00692900 · ClinicalTrials.gov registry record · Phase 1

Safety Study Involving Oxaliplatin With Docetaxel for Recurrent Ovarian,Primary Peritoneal, and Fallopian Tube Cancer

A Phase 1 study, sponsored by University of Pittsburgh.

Completed
Registry status
Phase 1
Development phase
25
Enrollment target

NCT00692900: Completed Phase 1 study, sponsored by University of Pittsburgh.

NCT00692900 is a Phase 1 study that has completed, run by University of Pittsburgh. The registered enrollment target is 25 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00692900, a Phase 1 study, has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
Phase 1
Development phase
25 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safest and maximum tolerated dosing regimens for intraperitoneal oxaliplatin with intravenous docetaxel and intravenous oxaliplatin with intraperitoneal docetaxel for recurrent ovarian, primary peritoneal, or fallopian tube cancer.

Interventions

  • DRUG intravenous docetaxel with intraperitoneal oxaliplatin
  • DRUG intravenous oxaliplatin with intraperitoneal docetaxel

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2008-12
Est. Completion 2013-10
Phase Phase 1
University of Pittsburgh

1,238 total trials

What the finished NCT00692900 record still lists

NCT00692900 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower).

The record links to 0 conditions, and to 2 interventions - of which intravenous docetaxel with intraperitoneal oxaliplatin is the first listed.

NCT00692900 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00692900 about?

NCT00692900 is a clinical study titled "Safety Study Involving Oxaliplatin With Docetaxel for Recurrent Ovarian,Primary Peritoneal, and Fallopian Tube Cancer". The purpose of this study is to determine the safest and maximum tolerated dosing regimens for intraperitoneal oxaliplatin with intravenous docetaxel and intravenous oxaliplatin with intraperitoneal docetaxel for recurrent ovarian, primary peritoneal, or fallopian tube cancer.

What is the current status of trial NCT00692900?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2008-12. Estimated completion is 2013-10.

What interventions are being tested in trial NCT00692900?

The interventions under investigation include: intravenous docetaxel with intraperitoneal oxaliplatin (DRUG), intravenous oxaliplatin with intraperitoneal docetaxel (DRUG).

Who is sponsoring clinical trial NCT00692900?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00692900's enrollment target sits among peer trials

25 1495th of 2000 higher than 481 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

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Source: ClinicalTrials.gov NCT00692900, the US trial registry maintained by the National Library of Medicine. NCT00692900 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.