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NCT00058071 · ClinicalTrials.gov registry record · Phase 3

Amifostine in Treating Peripheral Neuropathy in Patients Who Have Received Chemotherapy for Cancer

A Phase 3 study, sponsored by Gynecologic Oncology Group.

Completed
Registry status
Phase 3
Development phase
100
Enrollment target

NCT00058071 is a Phase 3 study that has completed, run by Gynecologic Oncology Group. The registered enrollment target is 100 participants.

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The verdict

NCT00058071, a Phase 3 study, has completed, sponsored by Gynecologic Oncology Group.

COMPLETED
Registry status
Phase 3
Development phase
100 participants
Enrollment target

Study Summary

RATIONALE: Amifostine may be effective in relieving numbness, tingling, and other symptoms of peripheral neuropathy. It is not yet known whether amifostine is effective in treating peripheral neuropathy in patients who have received chemotherapy for cancer. PURPOSE: This randomized phase III trial is studying amifostine to see how well it works compared to observation in relieving numbness, tingling, and other symptoms of peripheral neuropathy in patients who have received platinum-based chemotherapy (such as cisplatin or carboplatin) for cancer.

Interventions

  • DRUG amifostine trihydrate

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2003-03
Phase Phase 3

Sponsor

Gynecologic Oncology Group

154 total trials

What the Registry Record Tells You About NCT00058071

The ClinicalTrials.gov registry entry for NCT00058071 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gynecologic Oncology Group, which has 154 total studies on file at ClinicalTrials.gov.

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

NCT00058071 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00058071 about?

NCT00058071 is a clinical study titled "Amifostine in Treating Peripheral Neuropathy in Patients Who Have Received Chemotherapy for Cancer". RATIONALE: Amifostine may be effective in relieving numbness, tingling, and other symptoms of peripheral neuropathy. It is not yet known whether amifostine is effective in treating peripheral neuropathy in patients who have received chemotherapy for cancer. PURPOSE: This randomized phase III trial ...

What is the current status of trial NCT00058071?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 100 participants. The study started on 2003-03.

What interventions are being tested in trial NCT00058071?

The interventions under investigation include: amifostine trihydrate (DRUG).

Who is sponsoring clinical trial NCT00058071?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.