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NCT00003322 · ClinicalTrials.gov registry record · Phase 3

Combination Chemotherapy in Treating Patients With Primary Peritoneal or Stage III Epithelial Ovarian Cancer

A Phase 3 study, sponsored by Gynecologic Oncology Group.

Completed
Registry status
Phase 3
Development phase
384
Enrollment target

NCT00003322: Completed Phase 3 study, sponsored by Gynecologic Oncology Group.

NCT00003322 is a Phase 3 study that has completed, run by Gynecologic Oncology Group. The registered enrollment target is 384 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00003322, a Phase 3 study, has completed, sponsored by Gynecologic Oncology Group.

COMPLETED
Registry status
Phase 3
Development phase
384 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug and giving drugs in different ways may kill more tumor cells. It is not yet known whether intravenous two-drug combination chemotherapy is more effective than intravenous and intraperitoneal infusions of three-drug combination chemotherapy for treating primary peritoneal or stage III epithelial ovarian cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of intravenous two-drug combination chemotherapy with intravenous and intraperitoneal three-drug combination chemotherapy in treating patients who have primary peritoneal or stage III epithelial ovarian cancer.

Interventions

  • DRUG cisplatin
  • DRUG paclitaxel
  • PROCEDURE quality-of-life assessment

Trial Details

FieldValue
Enrollment Target 384 participants
Start Date 1998-03
Phase Phase 3
Gynecologic Oncology Group

154 total trials

What the finished NCT00003322 record still lists

NCT00003322 is an interventional study that assigns participants to a tested intervention. The registered 384 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 3 interventions - of which cisplatin is the first listed.

NCT00003322 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00003322 about?

NCT00003322 is a clinical study titled "Combination Chemotherapy in Treating Patients With Primary Peritoneal or Stage III Epithelial Ovarian Cancer". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug and giving drugs in different ways may kill more tumor cells. It is not yet known whether intravenous two-drug combination chemotherapy is more effecti...

What is the current status of trial NCT00003322?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 384 participants. The study started on 1998-03.

What interventions are being tested in trial NCT00003322?

The interventions under investigation include: cisplatin (DRUG), paclitaxel (DRUG), quality-of-life assessment (PROCEDURE).

Who is sponsoring clinical trial NCT00003322?

This trial is sponsored by Gynecologic Oncology Group, which has 154 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00003322's enrollment target sits among peer trials

384 975th of 2000 higher than 1,025 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT00003322, the US trial registry maintained by the National Library of Medicine. NCT00003322 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.