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

NCT ID: NCT01213654

Last Updated: 2010-10-04

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

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-04-30

Study Completion Date

2010-09-30

Brief Summary

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A pilot study to observe satisfaction of analgesia with intercostal catheters after VATS lobectomy.

Detailed Description

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

Conditions

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Lung Cancer Patients

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

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

\-

Exclusion Criteria

* do not understand DAnish
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Dept. of thoracic Surgery

AMBIG

Sponsor Role collaborator

Dept. of cardio-thoracic anaesthesia

AMBIG

Sponsor Role collaborator

Dept. Surgical PAthophysiology

AMBIG

Sponsor Role collaborator

all Blegdamsvej 9, 2100-Copenhagen, Denmark

UNKNOWN

Sponsor Role collaborator

Rigshospitalet, Denmark

OTHER

Sponsor Role lead

Responsible Party

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Section for Surgical Pathophysiology

Locations

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Rigshospitalet

Copenhagen, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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VATS-IC-2010

Identifier Type: -

Identifier Source: org_study_id