Yektas 2011.
Methods | RCT, 9 parallel groups |
Participants |
Number: 180 participants (9 × 20) Country: Turkey Surgery: inguinal surgery Age: 20 to 30 years ASA: I Other inclusion criteria: spinal anaesthesia Exclusion criteria: drug abuse, recall of pain at earlier surgery, need for additional sedation at earlier surgery, cerebrospinal fluid could not be obtained after 3 attempts, education level below primary school |
Interventions | Control group: 15 mg hyperbaric bupivacaine and 0.5 mL physiological serum intrathecally vs In the other groups, serum was replaced with the following to a total volume of 3.5 mL:
vs
vs
vs
vs
vs
vs
vs
|
Outcomes | Intraoperative and postoperative side effects Time to first pain |
Notes | Only abstract of conference paper available. Study authors contacted for additional information, awaiting reply |
RCT: randomized controlled trial; ASA: American Society of Anesthesiologists Physical Status 1 to 6, where 1 = Healthy person, 2 = Mild systemic disease, 3 = Severe systemic disease, 4 = Severe systemic disease that is a constant threat to life, 5 = A moribund person who is not expected to survive without the operation, 6 = A declared brain‐dead person whose organs are being removed for donor purposes; PCA: patient‐controlled analgesia; PACU: post‐anaesthesia care unit; BMI: body mass index