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

NCT00295945 · ClinicalTrials.gov registry record

Epidural Analgesia or Patient-Controlled Analgesia in Treating Patients Who Have Undergone Surgery for Gynecologic Cancer

A clinical trial, sponsored by University of California, San Francisco.

Completed
Registry status
240
Enrollment target

NCT00295945: Completed study, sponsored by University of California, San Francisco.

NCT00295945 is a clinical trial that has completed, run by University of California, San Francisco. The registered enrollment target is 240 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00295945 has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
240 participants
Enrollment target

Study Summary

RATIONALE: Giving pain medication into the space between the wall of the spinal canal and the covering of the spinal cord or giving it into a vein may help lessen pain caused by cancer surgery. It is not yet known whether epidural analgesia is more effective than patient-controlled analgesia in controlling pain in patients who have undergone surgery for gynecologic cancer. PURPOSE: This randomized clinical trial is studying epidural analgesia to see how well it works compared to patient-controlled analgesia in treating patients who have undergone surgery for gynecologic cancer.

Interventions

  • DRUG fentanyl citrate
  • DRUG hydromorphone hydrochloride
  • DRUG ropivacaine hydrochloride

Trial Details

FieldValue
Enrollment Target 240 participants
Start Date 2005-03
Est. Completion 2009-12

What the finished NCT00295945 record still lists

NCT00295945 is an observational study that tracks outcomes without assigning an intervention. The registered 240 participants enrollment target is mid-sized for trials with a published cap.

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

NCT00295945 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00295945 about?

NCT00295945 is a clinical study titled "Epidural Analgesia or Patient-Controlled Analgesia in Treating Patients Who Have Undergone Surgery for Gynecologic Cancer". RATIONALE: Giving pain medication into the space between the wall of the spinal canal and the covering of the spinal cord or giving it into a vein may help lessen pain caused by cancer surgery. It is not yet known whether epidural analgesia is more effective than patient-controlled analgesia in cont...

What is the current status of trial NCT00295945?

This trial is currently completed. The enrollment target is 240 participants. The study started on 2005-03. Estimated completion is 2009-12.

What interventions are being tested in trial NCT00295945?

The interventions under investigation include: fentanyl citrate (DRUG), hydromorphone hydrochloride (DRUG), ropivacaine hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00295945?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

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

  • NCT02855554 · 240 participants · NA

    Quantitative Cardiac Parametric Mapping

  • NCT03230565 · 240 participants · Phase 4

    Continuous Infusions vs Scheduled Bolus Infusions

  • NCT03399929 · 240 participants

    Traumatic Brain Injury and Stroke Long Term Outcome

  • NCT03583710 · 240 participants · Phase 3

    Mitotane With or Without Cisplatin and Etoposide After Surgery in Treating Patients With Stage I-III Adrenocortical Cancer With High Risk of Recurrence

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 NCT00295945, the US trial registry maintained by the National Library of Medicine. NCT00295945 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.