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NCT Number: NCT02674243

Efficacy of Iodopovidone Versus Talc in Palliative Malignant Pleural Effusion

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)

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Department of surgery, Faculty of medicine, Chiang Mai University Hospital

Chiang Mai, Chaing Mai, 50200, Thailand

About this study

Background and Rationale: Malignant pleural effusion (MPE) defined as presenting malignant cell in pleural effusion. It is usually found in advanced stage cancer or cancer of pleura. Most common primary tumor causing MPE is lung cancer (37%) followed with breast cancer (16%). From previous studies, when MPE was diagnosed, the median survival was only 3-12 months depending on primary tumor. In lung cancer, median survival for stage IV with MPE was only 4 months. However, quality of life of patient is also important. These patients should have less suffer from MPE. In recent era, chemotherapy, targeted therapy and immunotherapy are very useful for advanced stage cancer patients. They can prolong survival in such patients. Therefore, pleurodesis had role for palliative treatment hoping these patient have better quality of life. Talc (composed of oxygen, silicate, magnesium and carbon) has been used as one of common substances for chemical pleurodesis since 1935 by Norman Bethune with high efficacy (90%). However, it can cause a serious complication such as acute respiratory distress syndrome (ARDS). Although an incidence of ARDS is not too high, it can make patients died, therefore, other substances have been studied instead of using Talc. Iodopovidone has been one of interesting substances used as pleurodesis substance since 2006. It is low cost, and available. One meta-analysis of 13 observational studies with 499 patients found that iodopovidone was safe with success rate of pleurodesis was 70-100%. The most common side effect was chest pain. Previously, only two randomized control trial studies reported the efficacy of iodopovidone solution comparing to Talc for pleurodesis. They found that there were no statistical significant difference either efficacy or safety between two substances. The limitation of those studies is small sample size, therefore, we would like to compare the efficacy of iodopovidone solution for chemical pleurodesis with Talc.

Objectives: To compare the efficacy of Iodopovidone solution with Talc for pleurodesis in MPE Research methodology: This is a prospective randomized control trial. 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. Patients will be randomized to two groups; Iodopovidone group (intervention group) and Talc group (control group). The efficacy of both groups will be compared.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All MPE proved by cytology
  • After pleural effusion was released by chest tube drainage, lung was fully expanded

Exclusion criteria

  • Patients who have Karnofsky performance state ≤ 40
  • History of iodine allergy
  • History of morphine allergy
  • Abnormal thyroid hormones.

Treatment and study plan

Iodopovidone solution

Drug

In this group, iodopovidone solution will be used as pleurodesis substance

Other names: povidone-iodine solution

Talc

Drug

In this group, Talc will be used as pleurodesis substance

Other names: Talcum powder

Primary outcomes

  1. Success of treatment

    Time frame: 7 days

    Success of treatment defined as chest drain can be removed within 1 week after intervention

Secondary outcomes

  1. Amount of pleural effusion after pleurodesis

    Time frame: Until chest drain removal, an average of 7 days

    Observing amount of pleural effusion after intervention comparing between both groups

  2. Side effect

    Time frame: with 24 hours after intervention

    Side effects are chest pain, fever, and respiratory failure.

  3. Length of hospital stay

    Time frame: From date of randomization until the date of discharge or date of death from any cause, whichever came first, assessed up to 30 days

Sponsors and collaborators

Lead sponsor

Chiang Mai University

Other

Registry information

Official study title

Efficacy of Iodopovidone Versus Talc in Palliative Malignant Pleural Effusion: a Randomized Controlled Trial Study

Important dates

Study start
2015
Primary completion
2019
Study completion
2019
First posted
Feb 4, 2016
Registry last updated
Jan 23, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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