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Spinal Anesthesia in Total Hip Arthroplasty

NCT02818894 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 135

Last updated 2022-09-23

Study results available
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Summary

Spinal anesthesia is commonly used in patients undergoing total hip replacements. The purpose of this study is to compare lidocaine to bupivacaine spinal anesthesia in patients having a total hip arthroplasty (THA). The objective of this study is to compare the two spinal anesthesia treatments in regards to transient neurological symptoms (TNS).

Conditions

  • Total Hip Arthroplasty

Interventions

DRUG

Lidocaine

Spinal anesthesia administered prior to participant's THA

DRUG

Bupivacaine

Spinal anesthesia administered prior to participant's THA

Sponsors & Collaborators

  • Thomas L Bradbury

    lead OTHER

Principal Investigators

  • Thomas Bradbury, MD · Emory University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-27
Primary Completion
2020-03-05
Completion
2020-03-05
FDA Drug
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02818894 on ClinicalTrials.gov