Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00217633 · ClinicalTrials.gov registry record · Phase 2

Pelvic Exenteration in Treating Patients With Recurrent Cervical Cancer

A Phase 2 study, sponsored by Gynecologic Oncology Group.

Completed
Registry status
Phase 2
Development phase
38
Enrollment target

NCT00217633: Completed Phase 2 study, sponsored by Gynecologic Oncology Group.

NCT00217633 is a Phase 2 study that has completed, run by Gynecologic Oncology Group. The registered enrollment target is 38 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (71% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00217633, a Phase 2 study, has completed, sponsored by Gynecologic Oncology Group.

COMPLETED
Registry status
Phase 2
Development phase
38 participants
Enrollment target

Study Summary

This phase II trial is studying how well pelvic exenteration works in treating patients with recurrent cervical cancer. Pelvic exenteration may be effective in treating recurrent cervical cancer.

Interventions

  • PROCEDURE Conventional Surgery

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2006-01
Phase Phase 2
Gynecologic Oncology Group

154 total trials

What the finished NCT00217633 record still lists

NCT00217633 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 38 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (71% lower).

The record links to 0 conditions, and to 1 intervention - of which Conventional Surgery is the first listed.

NCT00217633 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00217633 about?

NCT00217633 is a clinical study titled "Pelvic Exenteration in Treating Patients With Recurrent Cervical Cancer". This phase II trial is studying how well pelvic exenteration works in treating patients with recurrent cervical cancer. Pelvic exenteration may be effective in treating recurrent cervical cancer.

What is the current status of trial NCT00217633?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 38 participants. The study started on 2006-01.

What interventions are being tested in trial NCT00217633?

The interventions under investigation include: Conventional Surgery (PROCEDURE).

Who is sponsoring clinical trial NCT00217633?

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 NCT00217633's enrollment target sits among peer trials

38 1467th of 2000 higher than 517 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01684904 · 38 participants · NA

    Proton Therapy for Esophageal Cancer

  • NCT03310879 · 38 participants · Phase 2

    Study of the CDK4/6 Inhibitor Abemaciclib in Solid Tumors Harboring Genetic Alterations in Genes Encoding D-Type Cyclins or Amplification of CDK4 or CDK6

  • NCT03896269 · 38 participants · Phase 1

    CPX-351 in Treating Patients With Relapsed or Refractory High Risk Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia

  • NCT04085315 · 38 participants · Phase 1

    Alisertib in Combination With Osimertinib in Metastatic EGFR-mutant Lung Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00217633, the US trial registry maintained by the National Library of Medicine. NCT00217633 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.