Anaesthesia
Conditions
Interventions
superior trunk group
upper thoracic erectore spinae block
Sponsors
menofia univeristy faculty of medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: • All patients of both sex within the age range from 18 to 70 years old. • Scheduled for elective arthroscopic shoulder surgery. • ASA I or II physical status
Exclusion criteria
Exclusion criteria: • Refusal of the patient informed consent. • Pre-existing neuropathy in the operated limb. • Coagulation disorders. • Neurological and/or psychological diseases. • Known allergy to local anesthetics, • Local infection at the puncture site • Pregnancy, breast-feeding. • BMI = 35 kg/m2
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is to measure and compare total analgesic consumption of both intraoperative and post operative opioids and non opioid drugs in ultrasound guided superior trunk block and ultrasound guided upper thoracic erector spinae plain block in patients undergoing shoulder arthroscopy | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes include comparing the efficacy of ultrasound-guided superior trunk block and ultrasound- guided high thoracic erector spinae plain block for postoperative analgesia management using a visual analogue scale (VAS) ranging from 0 (no pain) to 10 (worst imaginable pain). The patient will be asked to mark his pain level on this scale, VAS will be recorded in rest (static) and at mobilization (dynamic), on the ward, VAS scores will be recorded 1, 2, 4, 6, 12, and 24 hrs postoperatively, , effect of both block on surgical stress response, time to first rescue analgesia, block performance time, complications related to both blocks and adverse effect of used drugs, the patient satisfaction and time to discharge from hospital | — |
Countries
Egypt
Contacts
Public Contactamal Ismael abd elrahman
lecturer of anasethesia intensive care and pain managment
Outcome results
None listed