# Paravertebral Block for Improvement of Quality of Recovery Following Cardiac Surgery

> **NCT06008821** · NA · UNKNOWN · sponsor: **University of British Columbia** · enrollment: 224 (estimated)

## Conditions studied

- Post-operative Pain
- Post-cardiac Surgery
- Cardiac Disease

## Interventions

- **PROCEDURE:** Bilateral paravertebral block with 0.25% ropivicaine with 1:400,000 epinephrine
- **PROCEDURE:** Bilateral sham block with normal saline

## Key facts

- **NCT ID:** NCT06008821
- **Lead sponsor:** University of British Columbia
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2023-10-13
- **Primary completion:** 2025-11
- **Final completion:** 2025-11
- **Target enrollment:** 224 (ESTIMATED)
- **Last updated:** 2024-01-08

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06008821

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06008821, "Paravertebral Block for Improvement of Quality of Recovery Following Cardiac Surgery". Retrieved via AI Analytics 2026-07-26 from https://api.ai-analytics.org/clinical/NCT06008821. Licensed CC0.

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