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Clinical Trials/PACTR202402842689533
PACTR202402842689533
Recruiting
未知

Cervical Erector Spinae Plane Block versus Posterior Interscalene Brachial Plexus Block in Patients Undergoing Shoulder Arthroscopy: A Prospective Randomised Parallel Trial

Not provided0 sites80 target enrollmentJanuary 16, 2024
ConditionsAnaesthesia

Overview

Phase
未知
Intervention
Not specified
Conditions
Anaesthesia
Sponsor
Not provided
Enrollment
80
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 16, 2024
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Not provided

Eligibility Criteria

Inclusion Criteria

  • Patients aged 18–65 years
  • American Society of Anesthesiologists (ASA) I or II
  • Scheduled for elective unilateral shoulder arthroscopy (rotator cuff repair, bankart repair, superior labral tear from anterior to posterior repair, and/or acromioplasty).

Exclusion Criteria

  • Coagulation Or bleeding disorder, anticoagulant therapy
  • Cervical disc issues,
  • Allergy/sensitivity to local anaesthetics and/or opioids,
  • Infection in the block area,
  • Contralateral hemidiaphragmatic paralysis, pneumonectomy or vocal cord palsy, severe bronchopulmonary disease, including chronic obstructive pulmonary disease and obstructive sleep apnea.
  • Pregnancy or suspected pregnancy, breast feeding mother,
  • Body mass index greater than 35 kg/m2,
  • Significant psychiatric or cognitive conditions interfering with assessment.
  • Unstable coronary artery disease, congestive heart failure, or arrhythmias.
  • Pre\-existing neurological deficits or neuropathy affecting the brachial plexus. Cognitive or intellectual disability resulting in difficulty communicating with the care givers.

Outcomes

Primary Outcomes

Not specified

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