Effects of Desflurane and Propofol During Lung Volume Reduction Surgery

NCT ID: NCT04226625

Last Updated: 2020-01-13

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

PHASE4

Total Enrollment

18 participants

Study Classification

INTERVENTIONAL

Study Start Date

2000-01-31

Study Completion Date

2002-03-21

Brief Summary

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Patients presenting for lung volume reduction are very high risk patients and it is important they receive the best anesthetic available. This study aims to answer which is the best anesthetic for managing such cases.

Detailed Description

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The anesthetic technique for lung volume reduction surgery consists of a thoracic epidural in combination with a general anesthetic. The thoracic epidural is routine for this operation and allows administration of local anesthetics and painkillers in the epidural space which results in profound pain relief in the area of surgery. The epidural is routinely used for pain control during the surgery and after the surgery when the patient is awake.

The general anesthetic used may be a volatile agent (gas for example Desflurane), which is administered through the anesthesia machine, or an intravenous anesthetic agent, which is administered into a vein through an intravenous line as a continuous infusion (example Propofol). The use of an anesthetic agent and an epidural often causes a decrease in blood pressure which is treated with medication. The investigators are comparing the two anesthetic techniques regarding their effect on blood pressure and the amount of medication needed to treat it.

Conditions

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Lung Volume Reduction Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Patients were randomized to receive propofol or desflurane as the maintenance anesthetic.
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Propofol

Patients will receive Propofol as an intravenous (IV) agent, which is administered into a vein through an IV line as a continuous infusion.

Group Type ACTIVE_COMPARATOR

Propofol

Intervention Type DRUG

Intravenous administration

Desflurane

Patients will receive Desflurane as a gas that is administered through an anesthesia machine.

Group Type ACTIVE_COMPARATOR

Desflurane

Intervention Type DRUG

Volatile administration

Interventions

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Propofol

Intravenous administration

Intervention Type DRUG

Desflurane

Volatile administration

Intervention Type DRUG

Other Intervention Names

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Diprivan Suprane

Eligibility Criteria

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Inclusion Criteria

* Scheduled to undergo lung volume reduction surgery (LVRS)

Exclusion Criteria

* Does not sign a study consent form
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Columbia University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Bessie Kachulis, MD

Role: PRINCIPAL_INVESTIGATOR

Columbia University

Locations

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Columbia University Irving Medical Center

New York, New York, United States

Site Status

Countries

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United States

Other Identifiers

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9340

Identifier Type: OTHER

Identifier Source: secondary_id

AAAR3687

Identifier Type: -

Identifier Source: org_study_id

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