NCT Number: NCT00132613
Trial of Drainage With or Without Bleomycin Instillation for Malignant Pericardial Effusion
The purpose of this study is to evaluate the efficacy of pericardial instillation of bleomycin as a sclerosing agent after pericardial drainage for lung cancer-associated malignant pericardial effusion.
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Notify MeKey information
Conditions
Age range
Up to 75 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Aichi Cancer Center Hospital, Nagoya,Chikusa-ku,Kanokoden,1-1, Aichi-ken, Japan
About this study
Malignant pericardial effusions (MPEs), which are commonly associated with cardiac tamponade, make oncologic emergencies requiring prompt drainage. In lung cancer patients, MPE is one of the most unpleasant terminal events. Drainage usually results in prompt palliation of symptoms, but recurrent effusions often occur. Sclerosis with pericardial instillation of various agents is reported to prevent the recurrence, and bleomycin is the most commonly used drug, with fewer toxicities compared with others. There is, however, no prospective trial of pericardial sclerosis as compared with drainage alone for MPEs, and it is far from clear whether sclerosis really benefits these patients in terminal stages.
Comparison: Intra-pericardial instillation of bleomycin after pericardial drainage versus drainage alone for MPEs caused by lung cancer.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Pathologically documented lung cancer
- Clinically stable condition after pericardial drainage for malignant pericardial effusion (not necessary that it be documented by cytology)
- Expected to live 6 weeks or longer
- Sufficient organ function
- Signed informed consent
Exclusion criteria
- Myocardial infarction or unstable angina within 3 months
- Constrictive pericarditis
- Active pneumonitis
- Severe infection or disseminated intravascular coagulation (DIC)
- Other severe co-morbidity which could not be relieved with pericardial drainage
- Chemotherapy-naive small cell lung cancer
Treatment and study plan
Pericardial instillation of bleomycin after drainage
DrugPrimary outcomes
-
Survival without pericardial effusion at 2 months
Secondary outcomes
-
Successful extubation of pericardial drainage tube
-
time to extubation
-
survival without pericardial effusion at 1, 2, 4, 6, 12 months
-
symptom palliation
-
complication
-
long-term (> 6 months) effect on cardiac function
Sponsors and collaborators
Lead sponsor
Japan Clinical Oncology Group
Other
Collaborators
- Ministry of Health, Labour and Welfare, Japan
Registry information
Official study title
A Randomized Controlled Trial to Evaluate the Efficacy of Intra-pericardial Instillation of a Sclerosing Agent After Pericardial Drainage in Patients With Malignant Pericardial Effusion Associated With Lung Cancer (JCOG9811)
Important dates
- Study start
- 1999
- Primary completion
- 2006
- Study completion
- 2006
- First posted
- Aug 22, 2005
- Registry last updated
- Sep 22, 2016
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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