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OpenTrials
Completed

NCT Number: NCT03111797

Robot-assisted Lobectomy Versus Video-assisted Lobectomy

This prospective and observational cohort studies the morphine consumption difference during the first 48 hours after a lung lobectomy between patients operated with a robot assisted or a video-assisted technique for a lung cancer lobectomy.

Second outcome was to search eventual cardiac output difference during the surgery in 100 patients (50 in each group) using a non invasive monitoring device of cardiac output

All patients operated between january 2016 and March 2017 for a lung cancer lobectomy were included.

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Key information

Conditions

Robotic Surgical Procedures Agnosia Anesthesia and Analgesia Cardiac Output Nervous System Diseases Neurobehavioral Manifestations Neurologic Manifestations Pathological Conditions, Signs and Symptoms Perceptual Disorders Pneumonectomy; Status Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Departement anesthesie reanimation hopital nord

Marseille, 13015, France

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Volunteers
  • Mono lobectomy of lung for early stage cancer (T2Nx and earlier)
  • Video or robot assisted procedure

Exclusion criteria

  • Advanced stage of cancer (T3Nx and greater)
  • Need of thoracotomy conversion during procedure
  • Morphine intolerance or addiction.

Treatment and study plan

Morphine

Drug

we observe the self-patient controlled morphine consumption during the first 48h after surgery

Cardiac output measure

Other

we observe the cardiac output during surgical procedure using a non-invasive cardiac output monitoring device (ClearSight from Edwards lifescience laboratory )

Primary outcomes

  1. Morphine consumption

    Time frame: 48 hours after surgery

    morphine consumption for each patient using a self patient - controled morphine pump

Secondary outcomes

  1. cardiac output

    Time frame: during 30 minutes after incision and optic introduction

    continuous cardiac output during surgery procedure

Sponsors and collaborators

Lead sponsor

Hospital Nord

Other

Collaborators

  • Gary DUCLOS (Medical Doctor, investigator)

Registry information

Official study title

Robot-assisted Lobectomy Versus Video-assisted Lobectomy : a Prospective Observational Study

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Apr 13, 2017
Registry last updated
Apr 22, 2020

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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