hip fracture
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: over 60 years old age; both genders; physical status ASA II and ASA III; with transtrochanteric; subtrochanteric; acetabular and femoral fractures
Exclusion criteria
Exclusion criteria: Hypersensitivity to any of the drugs used in the study; need to use vasoactive drugs; ventilatory support; decompensated diabetes mellitus; severe arterial hypertension; previous or current coronary artery disease; previous or current stroke; blockade advanced cardiac; severe left ventricular dysfunction; renal or hepatic failure; intracranial hypertension; severe head trauma; glaucoma; psychiatric illness; illicit drugs users; patients who could not collaborate with the postoperative evaluation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement of pain during positioning (sitting) to perform spinal anesthesia, assessed by the visual analogue scale (0-10) after analgesic block, compared with venous opioid;Pain improvement in the first 24 hours of the postoperative period, assessed by the visual analogue scale (0-10), after analgesic block, comparing with venous opioid | — |
Countries
Brazil