Clinical Trials Directory

Trials / Terminated

TerminatedNCT00215748

Reduced Dexamethasone Pre-Medication Dose in Elderly Patients Receiving Weekly Docetaxel

Feasibility of A Reduced Dexamethasone Pre-Medication Dose in Elderly Patients Treated With Weekly Docetaxel

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Geriatric Oncology Consortium · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

Summary

This study is to explore the feasibility of an alternative dose of dexamethasone pre-medication in older breast and lung cancer patients who are receiving weekly docetaxel chemotherapy.

Detailed description

Dose-limiting edema and effusions associated with cumulative docetaxel administraton have necessitated the recommendation that all patients should be premedicated with oral corticosteroids such as dexamethasone prior to docetaxel administration. Dexamethasone pre-medication may also decrease the incidence and severity of acute hypersensitivity reactions associated with docetaxel administration. However, administration of weekly dexamethasone can cause additional untoward side effects, especially in the older population. If the data from this phase II study is encouraging, a study to evaluate an even lower dose of dexamethasone can be conducted.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasone

Timeline

Start date
2004-08-01
Completion
2007-04-01
First posted
2005-09-22
Last updated
2007-11-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00215748. Inclusion in this directory is not an endorsement.