drugset / Trial / NCT02674243

Efficacy of Iodopovidone Versus Talc in Palliative Malignant Pleural Effusion

NCT02674243

Phase 3 Completed 60 enrolled Chiang Mai University
RandomizedParallel-groupSingle-blindTreatment

Summary

This is prospective randomized control trial study. The aim of this study is to evaluate the efficacy of Iodopovidone solution for pleurodesis in palliative malignant pleural effusion (MPE) patients comparing to Talc. All adult patients who diagnosed MPE by cytology regardless primary tumor between December 1, 2015 and November 29, 2016 at Maharaj Nakorn Chiang Mai Hospital, Chiang Mai University, Chiang Mai, Thailand will be enrolled in this study. The inform and consent will be applied in all patients before treatment. Patients will be randomized to two groups; Iodopovidone group (intervention group) and Talc group (control group)

Timeline

Start
2015-11
Primary completion
2019-12
Completion
2019-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Iodopovidone Unknown
Comparator TALC ANHYDROUS Small molecule

Indications