CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 92 enrolled
Drug / intervention
PIOGLITAZONE VS. PLACEBO 30 mg +2 moredrug
Likely dose
PIOGLITAZONE VS. PLACEBO 30 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00780234
NCT00780234Phase 2Completed

Pioglitazone for Lung Cancer Chemoprevention

VA Office of Research and Development·interventional·Posted Oct 27, 2008·Updated Apr 11, 2019

In Brief

A Phase 2 clinical trial evaluating fluorescence bronchoscopy, quantitative high resolution CT scan, and 1 other intervention for Lung Cancer and Endobronchial Dysplasia. Completed, enrolled 92 participants across 2 sites.

Detailed Summary

This is a chemoprevention trial evaluating the diabetic agent pioglitazone. Non-diabetic subjects at risk for lung cancer (based on smoking history, lung function testing, and atypical cells in a sputum sample) receive either placebo or pioglitazone and have chest computerized tomography (CAT) scans and examinations of their airways with a bronchoscope at the start of the trial and after 6 months on treatment. Compensation will be provided to the subject after completing the trial.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedOct 27, 2008
Enrollment StartAug 1, 2009
Primary CompletionJun 1, 2016
Study CompletionAug 1, 2017
TodayJul 2, 2026
Enrollment to primary: 6.8 yearsPosted 17.7 years ago

Interventions

fluorescence bronchoscopyprocedure

examination of the central airways with a bronchoscope. Both white light and fluorescent light will be used.

quantitative high resolution CT scanprocedure

High resolution CT scan of the chest

PIOGLITAZONE VS. PLACEBO 30 mgdrug

Patients will be randomized to receive either pioglitazone or placebo. Pioglitazone hydrochloride, a thiazolidinedione antidiabetic agent and a potent peroxisome proliferator- activated receptor-gamma agonist. It is FDA approved for the treatment of Type II diabetes. It has been previously administered to non-diabetic subjects. The most common side effect of pioglitazone is fluid retention and modest weight gain. There is a potential risk that pioglitazone may cause an elevation in liver enzymes and more serious hepatotoxicity (rare). There is risk of edema and weight gain associated with pioglitazone therapy. 5% experienced peripheral edema in clinical trials. fluid retention may result in new onset heart failure or exacerbation of existing heart failure. Small risk of hypoglycemia, anemia, myalgia, bone fracture, headache, and macular retinal edema exists. There is insufficient information to confirm its safety in Pregnancy/Breastfeeding. Bladder cancer is more serious but rare.