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The Effect of Paravertebral Block Using a Multi-orifice Catheter on Preventing Acute and Chronic Post-thoracotomy Pain

CompletedNot applicableNCT01039870
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This study aims to evaluate the effect of the paravertebral block using a multi-lumen catheter on the incidence and severity of acute and chronic postthoracotomy pain compared to the thoracic epidural block.

Study details

Conditions
  • Acute Postthoracotomy Pain
  • Chronic Postthoracotomy Pain
  • Hypotension After Bolus Dose
Interventions
  • Procedure: paravertebral block
  • Procedure: thoracic epidural analgesia
Sponsor
Seoul National University Hospital
Start date
2010-07
Primary completion
2012-02
Sex
All
Age range
from 19 Years to 80 Years
Results posted
No results posted in this snapshot
Countries
South Korea
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * patients receiving surgery through a thoracotomy incision Exclusion Criteria: * patients with cardiovascular disease * patients with neurologic disease * patients with contraindications to paravertebral block or epidural block * patients with history of previous thoracotomy incision * patients with pain at the expected incision site

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01039870