Clinical Trials Directory

Trials / Completed

CompletedNCT00031785

Megestrol in Treating Patients Who Are Undergoing Radiation Therapy for Lung Cancer

A Phase III, Double-Blind, Randomized Study of the Effect of Megestrol Acetate on Weight and Health Related Quality of Life in Lung Cancer Patients Receiving Thoracic Radiation Therapy

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
25 (actual)
Sponsor
Wake Forest University Health Sciences · Academic / Other
Sex
All
Age
18 Years – 120 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Megestrol helps improve appetite. It is not yet known if megestrol is effective in limiting weight loss in patients who are undergoing radiation therapy. PURPOSE: Randomized phase III trial to determine the effectiveness of megestrol in limiting weight loss in patients who are undergoing radiation therapy for lung cancer.

Detailed description

OBJECTIVES: * Determine the effect of megestrol on weight in patients receiving radiotherapy for lung cancer. * Determine the quality of life of patients treated with this drug. OUTLINE: This is a randomized, placebo-controlled, double-blind, multicenter study. Patients are stratified according to histology (non-small cell lung cancer vs small cell lung cancer), and type of treatment (radiotherapy vs radiotherapy and non-cisplatin-containing chemotherapy vs radiotherapy and cisplatin-containing chemotherapy). Patients are randomized to one of two treatment arms. All patients undergo thoracic radiotherapy beginning on week 1 and continuing for a total of 5-7 weeks. * Arm I: Patients receive oral megestrol once daily beginning within the first 3 days of radiotherapy and continuing until 12 weeks after the completion of radiotherapy. * Arm II: Patients receive oral placebo once daily beginning within the first 3 days of radiotherapy and continuing until 12 weeks after the completion of radiotherapy. In both arms, quality of life is assessed at baseline, at the completion of radiotherapy, and at 4, 8, 12, 16, and 20 weeks after the completion of radiotherapy. Patients are followed at 4 and 8 weeks. PROJECTED ACCRUAL: A total of 98 patients (49 per treatment arm) will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGmegestrol acetate
RADIATIONradiation therapy

Timeline

Start date
2000-09-01
Primary completion
2002-09-11
Completion
2002-09-11
First posted
2003-08-06
Last updated
2021-09-09

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT00031785. Inclusion in this directory is not an endorsement.