The First Therapeutic Intervention in Malignant Pleural Effusion Trial
NCT ID: NCT00896285
Last Updated: 2015-07-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
4 participants
INTERVENTIONAL
2009-04-30
2014-12-31
Brief Summary
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The investigators hope to find the best way to prevent pain during pleurodesis.
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Detailed Description
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This trial is looking at which of two different drug regimens is more effective in preventing pleurodesis pain, and whether the size of chest tube influences pain. It will also address whether either of these influences success rate of pleurodesis.
We hope to learn whether the size of chest drain or the type of pain medication given (ibuprofen or morphine) influences the amount of pain felt after the pleurodesis procedure. We hope to find the best way of preventing pain during this procedure.
Conditions
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Study Design
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RANDOMIZED
FACTORIAL
SUPPORTIVE_CARE
NONE
Study Groups
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1
Large bore chest drain + NSAID based analgesic regimen
Chest tube greater than 14 French size and ibuprofen.
2
Small bore chest drain + NSAID based analgesic regimen
Chest tube less than or equal to 14 French size and ibuprofen.
3
Large bore chest drain + opiate based analgesic regimen
Chest tube greater than 14 French size and morphine.
4
Small bore chest drain + opiate based analgesic regimen
Chest tube less than or equal to 14 French size and morphine.
Interventions
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Large bore chest drain + NSAID based analgesic regimen
Chest tube greater than 14 French size and ibuprofen.
Small bore chest drain + NSAID based analgesic regimen
Chest tube less than or equal to 14 French size and ibuprofen.
Large bore chest drain + opiate based analgesic regimen
Chest tube greater than 14 French size and morphine.
Small bore chest drain + opiate based analgesic regimen
Chest tube less than or equal to 14 French size and morphine.
Eligibility Criteria
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Inclusion Criteria
* Histologically proven pleural malignancy OR
* Typical features of pleural malignancy seen on direct vision during thoracoscopy OR
* Pleural effusion in the context of histologically proven cancer elsewhere
2. Expected survival more than 1 month
3. Written informed consent
Exclusion Criteria
2. Primary lymphoma or small cell lung carcinoma
3. Patients who are pregnant or lactating
4. Inability to give informed consent
5. History of GI bleeding or of untreated peptic ulceration
6. Known sensitivity to non-steroidal anti-inflammatory drugs (NSAIDs)/opiates/acetaminophen
7. Hypercapnic respiratory failure
8. Known intravenous drug abuse
9. Severe renal or liver disease
10. Known bleeding diathesis
11. Warfarin therapy
12. Current or recent (within 2 weeks) corticosteroid steroid therapy
18 Years
ALL
No
Sponsors
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University of California, Davis
OTHER
Responsible Party
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Principal Investigators
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RJO Davies, Dr.
Role: PRINCIPAL_INVESTIGATOR
Oxford Pleural Unit, Churchill Hospital, Oxford, England
Locations
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UC Davis Medical Center
Sacramento, California, United States
Countries
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Other Identifiers
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200816478
Identifier Type: -
Identifier Source: org_study_id
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