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Evaluation of the Clinical Efficacy and Safety of BriTurn Injection or BrisTurn Prefilled Injection

Evaluation of the Clinical Efficacy and Safety of BriTurn Injection or BrisTurn Prefilled Injection

Recruiting
19 years and older
All
Phase N/A
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  • Simplified (AI rewritten)

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Overview

This study evaluate clinical efficacy and safety in adult patients administered BriTurn injection or BrisTurn Prefilled injection for reversal of neuromuscular blockade induced by Rocuronium or Vecuronium.

Description

This study evaluate clinical efficacy and safety in adult patients administered BriTurn injection or BrisTurn Prefilled injection for reversal of neuromuscular blockade induced by Rocuronium or Vecuronium.

  • Efficacy: Time (minutes) for Train-Of-Four (TOF) ratio to reach 0.9 (90%)
  • Safety: whether bradycardia and resulting cardiac arrest occur or whether bronchospasm occurs

Eligibility

Inclusion Criteria:

  • Adults over 19 years of age
  • Subject administered BriTurn Injection or BrisTurn Prefilled Injection for reversal of neuromuscular blockade induced by Rocuronium or Vecuronium

Exclusion Criteria:

  • Pregnant women or nursing women
  • Subject to prohibition according to the permission of BriTurn Injection or BrisTurn Prefilled Injection

Study details
    Reversal of Neuromuscular Blockade

NCT06246331

Hanlim Pharm. Co., Ltd.

14 February 2024

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