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NCT00039442 · ClinicalTrials.gov registry record · Phase 2

Capecitabine in Treating Patients With Persistent or Recurrent Cervical Cancer

A Phase 2 study, sponsored by Gynecologic Oncology Group.

Completed
Registry status
Phase 2
Development phase
21
Enrollment target

NCT00039442: Completed Phase 2 study, sponsored by Gynecologic Oncology Group.

NCT00039442 is a Phase 2 study that has completed, run by Gynecologic Oncology Group. The registered enrollment target is 21 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00039442, a Phase 2 study, has completed, sponsored by Gynecologic Oncology Group.

COMPLETED
Registry status
Phase 2
Development phase
21 participants
Enrollment target

Study Summary

Phase II trial to study the effectiveness of capecitabine in treating patients who have persistent or recurrent cervical cancer. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.

Interventions

  • DRUG Capecitabine
  • OTHER Laboratory Biomarker Analysis

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2002-04-29
Phase Phase 2
Gynecologic Oncology Group

154 total trials

What the finished NCT00039442 record still lists

NCT00039442 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (84% lower).

The record links to 0 conditions, and to 2 interventions - of which Capecitabine is the first listed.

NCT00039442 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00039442 about?

NCT00039442 is a clinical study titled "Capecitabine in Treating Patients With Persistent or Recurrent Cervical Cancer". Phase II trial to study the effectiveness of capecitabine in treating patients who have persistent or recurrent cervical cancer. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.

What is the current status of trial NCT00039442?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 21 participants. The study started on 2002-04-29.

What interventions are being tested in trial NCT00039442?

The interventions under investigation include: Capecitabine (DRUG), Laboratory Biomarker Analysis (OTHER).

Who is sponsoring clinical trial NCT00039442?

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 NCT00039442's enrollment target sits among peer trials

21 1794th of 2000 higher than 196 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00039442, the US trial registry maintained by the National Library of Medicine. NCT00039442 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.