Spinals in THA (Total Hip Arthroplasty)
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Osteoarthritis
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Triple (Participant, Investigator, Outcomes Assessor)Primary Purpose: Supportive Care
Participation Requirements
- Age
- Between 18 years and 90 years
- Gender
- Both males and females
Description
Participants will have their patient records examined prospectively and complete up to four telephone questionnaires after randomization to lidocaine or bupivacaine spinal anesthesia to see how they are feeling after their total hip arthroplasty (THA). Transient neurological symptoms, urinary retent...
Participants will have their patient records examined prospectively and complete up to four telephone questionnaires after randomization to lidocaine or bupivacaine spinal anesthesia to see how they are feeling after their total hip arthroplasty (THA). Transient neurological symptoms, urinary retention, timing of full mobilization, incidence of hypotension, and length of hospital stay will be recorded for both methods of spinal anesthesia for comparison.
Tracking Information
- NCT #
- NCT02818894
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Thomas Bradbury, MD Emory University
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