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erve plexus block associated with spinal anesthesia without morphine for hip surgery: A comparative to spinal anesthesia with morphine

Phase 3
Conditions
Pertrocantheric hip fracture
subtrochanteric hip fracture
femoral neck fracture
acetabulum fracture
fracture of other parts of the femur
Registration Number
RBR-2h39fm9
Lead Sponsor
Hospital e Maternidade Marieta Konder Bornhausen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruitment completed
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

This study included patients who underwent elective or emergency surgery for hip fracture correction or hip prosthesis insertion, who voluntarily agreed to participate in this research, over 18 years old, with a score of 15 on the Glasgow Coma Scale, with ability to correctly answer the questionnaire applied by the researcher and who signed the informed consent form.

Exclusion Criteria

The patients excluded from this work were those who underwent emergency surgery; who reported allergy to local anesthetics (both ropivacaine and bupivacaine); who presented local skin infection where both spinal anesthesia and lumbar plexus block should be punctured were excluded from this study; severe coagulation disorder or use of anticoagulants not paused for adequate time; who had pathologies that prevented the positioning for performing lumbar plexus block or spinal anesthesia; who had neurological symptoms present at the site of innervation related to the lumbar plexus; who had hemodynamic instability; , defined in the study as systolic blood pressure less than 90 mmHg, heart rate greater than 110 beats per minute or need for vasoactive drugs; those who had intracranial hypertension or who were in the presence of sepsis

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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