The First Therapeutic Intervention in Malignant Pleural Effusion Trial

NCT ID: NCT00896285

Last Updated: 2015-07-20

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

4 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-04-30

Study Completion Date

2014-12-31

Brief Summary

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Fluid caused by cancer cells may accumulate in the lining of the lung. Draining the fluid with a chest tube may relieve pain and shortness of breath. To stop the fluid from coming back again, patients are given a medicine (talc) into the chest drain to seal up the space around the lung. This procedure is known as pleurodesis. This sometimes causes pain and discomfort, and the investigators do not know the best way of preventing this.

The investigators hope to find the best way to prevent pain during pleurodesis.

Detailed Description

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Patients with metastatic cancer often have fluid collecting around the lung as a result of cancer cells spreading to the membranes adjacent to the lung (malignant pleural effusion). The standard way of treating this condition, which may cause unpleasant symptoms such as breathlessness and cough, is to drain the fluid off and then seal the cavity, using a drug (talc) given into the chest drain. Talc causes inflammation in the lining of the lung and chest wall, sticking the two surfaces together and preventing fluid from recurring. This procedure is often very painful; the pain may be partly related to the size of the chest tube used and the type of analgesia taken by the patient during the procedure. Reducing the amount of pain associated with this procedure would be a substantial benefit for patients undergoing this procedure.

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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Malignant Pleural Effusion Pleural Effusion

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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1

Group Type ACTIVE_COMPARATOR

Large bore chest drain + NSAID based analgesic regimen

Intervention Type OTHER

Chest tube greater than 14 French size and ibuprofen.

2

Group Type ACTIVE_COMPARATOR

Small bore chest drain + NSAID based analgesic regimen

Intervention Type OTHER

Chest tube less than or equal to 14 French size and ibuprofen.

3

Group Type ACTIVE_COMPARATOR

Large bore chest drain + opiate based analgesic regimen

Intervention Type OTHER

Chest tube greater than 14 French size and morphine.

4

Group Type ACTIVE_COMPARATOR

Small bore chest drain + opiate based analgesic regimen

Intervention Type OTHER

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.

Intervention Type OTHER

Small bore chest drain + NSAID based analgesic regimen

Chest tube less than or equal to 14 French size and ibuprofen.

Intervention Type OTHER

Large bore chest drain + opiate based analgesic regimen

Chest tube greater than 14 French size and morphine.

Intervention Type OTHER

Small bore chest drain + opiate based analgesic regimen

Chest tube less than or equal to 14 French size and morphine.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Clinically confident diagnosis of malignant pleural effusion requiring pleurodesis. The diagnosis may be established by one of:

* 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

1. Age \< 18 years
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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of California, Davis

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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United States

Other Identifiers

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200816478

Identifier Type: -

Identifier Source: org_study_id

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