MedPath

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

Completed
Conditions
Lung Cancer Patients
Registration Number
NCT01213654
Lead Sponsor
Rigshospitalet, Denmark
Brief Summary

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

Detailed Description

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

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria

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

Exclusion Criteria
  • do not understand DAnish

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
NRS (pain score 0-10))Until discharge (2-4 days)

Painscore

satisfaction (Verbal ranking scale 1-4)until discharge, 2-4 days

qualitative measurement

Secondary Outcome Measures
NameTimeMethod
Side effects (quantitatively, see details)until discharge, 2-4 days

Daily presence of, Nausea Dizziness Vomiting Sedation Pruritus

Trial Locations

Locations (1)

Rigshospitalet

🇩🇰

Copenhagen, Denmark

© Copyright 2025. All Rights Reserved by MedPath