The effect of lateral pectoral nerve block in combination with interscalene nerve block on opioid consumption and pain on awake shoulder arthroscopy patients

Phase 1

• Conditions: Peri- and postoperative pain after shoulder arthroscopy; MedDRA version: 20.0Level: LLTClassification code 10077421Term: Shoulder arthroscopySystem Organ Class: 100000004848; Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]

• Registration Number: EUCTR2022-000093-25-DK
• Lead Sponsor: Aarhus University Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-01-31
• Last Update Posted: 16 May 2022

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

• Set for elective shoulder arthroscopy by one single orthopedic surgeon
• Planned acromioclavikular decompression
• Planned awake surgery anesthetized by an interscalene nerve block
• ASA I-III
• Patient = 18 years
• Informed consent

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 12
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 12

Exclusion Criteria

• Inability to cooperate
• Unable to speak and/or understand danish or other types of communication problems
• Other major planned operative procedures planned during this operation (Bankart, cuff-operations etc.)
• Allergy to local analgesics in the study (Marcain + adrenaline)
• Lack of tolerance of Fentanyl
• Chronic pain with daily opioid consumption (dosed > x 1 day)
• Chronic pain treated with gabapentin, pregabalin, tricyclic antidepressants, opioid antagonists or SNRI
• Treatment with antipsychotics
• The patient is unsuitable for awake surgery
• Known abuse of alcohol, drugs or medicine
• Previous shoulder surgery on the planned side for this shoulder arthroscopy
• Previous participation in this study
• Pregnancy

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified