Postoperative Pain After Knee Arthroscopy
Conditions
Keywords
pregabalin, adductor canal block, postoperative pain
Brief summary
arthroscopically Anterior Cruciate Ligament Reconstruction (ACL) under spinal anesthesia were included in this study.
Detailed description
Patients who American Society of Anesthesiologists (ASA) classification I to II scheduled to undergo arthroscopically assisted ACL reconstructions under spinal anesthesia are included in this study. The first group is administered 150 mg oral pregabalin 1 hour before surgery and the postoperative sham block was performed with an ultrasound probe. The second group is the control group; patients in this group are administered a placebo capsule 1 hour before surgery and sham block was performed with an ultrasound probe.The third group is administered a placebo capsule 1 hour before surgery and postoperative adductor canal block is performed. All patients will be received postoperative a tramadol i.v. patient control analgesia device. At the end of 24 hours, the total amount of tramadol consumed by the patient will be recorded from the patient control analgesia. NRS score, white fast track, satisfaction will be questioned.
Interventions
preoperative pregabalin and the postoperative sham block will perform.
DRUGPlacebo oral tablet
The preoperative placebo oral tablet and the postoperative sham block will perform.
DRUGadductor canal block including bupivacaine
The preoperative placebo oral tablet and adductor channel block including 10 mL of 0.25% bupivacaine with 5 μg/mL epinephrine
Sponsors
Ankara Diskapi Training and Research Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
* Patients between the ages of 18 and 70 years * American Society of Anesthesiologists I or II * Scheduled to undergo knee arthroscopy
Exclusion criteria
* allergic to any medicines * History of drug or alcohol abuse, * Opioids or sedative medications * History of psychiatric conditions * Pregnant or lactating women
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 11-point numerical rating scale (NRS) | 24 hours | 11-point numerical rating scale for pain (0='no pain' and 10='worst pain possible pain') were explained. |
| tramadol consumption | 24 hours | 24 hours tramadol consumption will be recorded as milligrams |
Countries
Turkey (Türkiye)
Outcome results
None listed