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Completed

NCT Number: NCT00896285

The First Therapeutic Intervention in Malignant Pleural Effusion Trial

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UC Davis Medical Center

Sacramento, California, 95817, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 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
  • Expected survival more than 1 month
  • Written informed consent

Exclusion criteria

  • Age < 18 years
  • Primary lymphoma or small cell lung carcinoma
  • Patients who are pregnant or lactating
  • Inability to give informed consent
  • History of GI bleeding or of untreated peptic ulceration
  • Known sensitivity to non-steroidal anti-inflammatory drugs (NSAIDs)/opiates/acetaminophen
  • Hypercapnic respiratory failure
  • Known intravenous drug abuse
  • Severe renal or liver disease
  • Known bleeding diathesis
  • Warfarin therapy
  • Current or recent (within 2 weeks) corticosteroid steroid therapy

Treatment and study plan

Large bore chest drain + NSAID based analgesic regimen

Other

Chest tube greater than 14 French size and ibuprofen.

Small bore chest drain + NSAID based analgesic regimen

Other

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

Large bore chest drain + opiate based analgesic regimen

Other

Chest tube greater than 14 French size and morphine.

Small bore chest drain + opiate based analgesic regimen

Other

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

Primary outcomes

  1. An average pain score over 72 hours post pleurodesis for malignant pleural effusion

    Time frame: 72 hours

  2. Pleurodesis success at 3 months post randomization (time to relapse of pleural effusion)

    Time frame: 3 months

Secondary outcomes

  1. Presence of chronic chest pain on the side of the pleurodesis

    Time frame: 6 weeks

  2. Presence of chronic chest pain on the side of the pleurodesis

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

University of California, Davis

Other

Registry information

Official study title

TIME1: A 2 X 2 Factorial Trial to Assess Whether Non-steroidal Anti-inflammatory Analgesics and Small-bore Chest Tubes Are Less Painful Than Opiate Analgesics and Large-bore Chest Tubes in Pleurodesis for Malignant Pleural Effusion.

Acronym: TIME-1

Important dates

Study start
2009
Primary completion
2014
Study completion
2014
First posted
May 11, 2009
Registry last updated
Jul 20, 2015

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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