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NCT06833086

Influence of Thoracic Paravertebral Block on Atrioventricular Conduction

Completed Last updated 3 April 2025
What this trial tests

trial testing Paravertebral block (ropivacaine) left in Conduction Abnormalities in 60 participants. Completed in 31 March 2025.

Timeline
20 February 2025
Primary endpoint
31 March 2025
31 March 2025

Quick facts

Lead sponsorMedical University of Gdansk
StatusCompleted
Study typeOBSERVATIONAL
Enrollment60
Start date20 February 2025
Primary completion31 March 2025
Estimated completion31 March 2025
Sites1 location across Poland

Drugs / interventions tested

Conditions studied

Sponsor

Medical University of Gdansk

Who can join

18 and older, female only, with Conduction Abnormalities or Paravertebral Anesthesia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study is to assess the changes in electrical activity of heart atria and in atrioventricular conduction induced by anaesthetic thoracic paravertebral blockade, depending on site on which blockade was performed. Researchers will retrospectively compare ECG recordings of patients that undergone unilateral paravertebral blockade at T3 level with 0.5% ropivacaine. The investigation will include measurement of P wave and PR interval, and subsequent statystical analysis.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Paravertebral block (ropivacaine) left

Trials testing the same drug.

Other Medical University of Gdansk trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06833086.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing