Postoperative Analgesia Clinical Trial
Official title:
The Effect of Adding Dexamethasone to Bupivacaine in Ultrasound Guided Adductor Canal Block for Postoperative Analgesia Following Knee Arthroscopic Anterior Cruciate Ligament Reconstruction
The purpose of this study was to evaluate the efficacy of ultra-sound guided adductor canal block with and without dexamethasone when added to bupivacaine on the duration of postoperative analgesia in patients undergoing arthroscopic anterior cruciate ligament reconstruction surgery using Numeric Rating Score (NRS).
Adductor canal block was done by Ultra-sound. After confirmation of the block and exclusion
of any signs of toxicity or nerve injury, the patients operations were done under spinal
anesthesia. Patients were allocated into one of 2 groups (30 patients per group).
I. Group I: the patients received a single-shot of 20 ml plain bupivacaine (0.5%) +2 ml
normal saline.
ii.Group II: the patients received 20ml plain bupivacaine (0.5%) + 8 mg dexamethasone (2ml).
Postoperative pain were assessed by Numeric Rating Scale (N.R.S) every 6 h post-operatively
for 24 h.
Whenever, the NRS Score was ≥4 or the patient requested pain medication, analgesia was
provided by ketorolac 30 mg amp IV, then morphine 1mg ̸ kg slowly IV as a rescue analgesia.
Time to first request for analgesia & total dose of rescue analgesia were be recorded.
10. Satisfaction score will be measured on a linear numerical scale; ranging from 0 =
complete dissatisfaction to 10 = complete satisfaction. Any post-operative side effects, like
nausea, vomiting, bradycardia, hypotension will be also documented. The time to first
analgesic requirement will be recorded, and the cumulative, post-operative opioid consumption
in 24 h post-operatively will be recorded. Assessment of Quadriceps Strength at preoperative,
6, 12, 18, and 24 h postoperative from zero to 5.
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