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Inter Costal Catheters for Video-Assisted Thoroscopic (VATS) Lobectomy

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ClinicalTrials.gov Identifier: NCT01213654
Recruitment Status : Completed
First Posted : October 4, 2010
Last Update Posted : October 4, 2010
Sponsor:
Collaborators:
Information provided by:

Study Description
Brief Summary:
A pilot study to observe satisfaction of analgesia with intercostal catheters after VATS lobectomy.

Condition or disease
Lung Cancer Patients

Detailed Description:
Pain and satisfaction with pain treatment is investigated in a population after VATS lobectomy.

Study Design

Study Type : Observational
Actual Enrollment : 50 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Pain Relief After VATS Lobectomy Using Interoperatively Placed Inter Costal Catheters.
Study Start Date : April 2010
Primary Completion Date : September 2010
Study Completion Date : September 2010

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Groups and Cohorts


Outcome Measures

Primary Outcome Measures :
  1. NRS (pain score 0-10)) [ Time Frame: Until discharge (2-4 days) ]
    Painscore

  2. satisfaction (Verbal ranking scale 1-4) [ Time Frame: until discharge, 2-4 days ]
    qualitative measurement


Secondary Outcome Measures :
  1. Side effects (quantitatively, see details) [ Time Frame: until discharge, 2-4 days ]
    Daily presence of, Nausea Dizziness Vomiting Sedation Pruritus


Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Consenting lung cancer patients due for elective surgery
Criteria

Inclusion Criteria:

Age of consent (ie age>=18) Eligible for lobectomy Able to comply Willing to register postoperatively

Exclusion Criteria:

  • do not understand DAnish
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01213654


Locations
Denmark
Rigshospitalet
Copenhagen, Denmark, 2100
Sponsors and Collaborators
Rigshospitalet, Denmark
Dept. of thoracic Surgery
Dept. of cardio-thoracic anaesthesia
Dept. Surgical PAthophysiology
all Blegdamsvej 9, 2100-Copenhagen, Denmark
More Information

Responsible Party: MD Kim Wildgaard, Section for Surgical Pathophysiology
ClinicalTrials.gov Identifier: NCT01213654     History of Changes
Other Study ID Numbers: VATS-IC-2010
First Posted: October 4, 2010    Key Record Dates
Last Update Posted: October 4, 2010
Last Verified: October 2010

Keywords provided by Rigshospitalet, Denmark:
Lung cancer
VATS Lobectomy