Viewing Study NCT00041093


Ignite Creation Date: 2025-12-25 @ 1:22 AM
Ignite Modification Date: 2026-01-01 @ 9:22 PM
Study NCT ID: NCT00041093
Status: COMPLETED
Last Update Posted: 2018-01-10
First Post: 2002-07-08
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Docetaxel in Treating Patients With Persistent or Recurrent Cervical Cancer
Sponsor: Gynecologic Oncology Group
Organization:

Study Overview

Official Title: A Phase II Evaluation Of Docetaxel (NSC #628503) In The Treatment Of Persistent Or Recurrent Squamous Cell Carcinoma Of The Cervix
Status: COMPLETED
Status Verified Date: 2018-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Phase II trial to study the effectiveness of docetaxel 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.
Detailed Description: PRIMARY OBJECTIVES:

I. Determine the antitumor activity of docetaxel in patients with persistent or recurrent squamous cell carcinoma of the cervix.

II. Determine the toxicity of this drug in these patients.

OUTLINE: This is a multicenter study.

Patients receive docetaxel IV over 1 hour on day 1. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Patients are followed every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter.

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
NCI-2012-02476 REGISTRY CTRP (Clinical Trial Reporting Program) View
CDR0000069442 None None View
GOG-0127S OTHER Gynecologic Oncology Group View
GOG-0127S OTHER CTEP View
U10CA027469 NIH None https://reporter.nih.gov/quic… View