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Completed

NCT Number: NCT01213654

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

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Rigshospitalet

Copenhagen, 2100, Denmark

About this study

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

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

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

-

Exclusion criteria

  • do not understand DAnish

Treatment and study plan

Primary outcomes

  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 outcomes

  1. Side effects (quantitatively, see details)

    Time frame: until discharge, 2-4 days

    Daily presence of, Nausea Dizziness Vomiting Sedation Pruritus

Sponsors and collaborators

Lead sponsor

Rigshospitalet, Denmark

Other

Collaborators

  • Dept. Surgical PAthophysiology
  • Dept. of cardio-thoracic anaesthesia
  • Dept. of thoracic Surgery
  • all Blegdamsvej 9, 2100-Copenhagen, Denmark

Registry information

Official study title

Pain Relief After VATS Lobectomy Using Interoperatively Placed Inter Costal Catheters.

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Oct 4, 2010
Registry last updated
Oct 4, 2010

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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