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临床试验/NCT06747494
NCT06747494
招募中
不适用

General Versus Spinal Anesthesia for Total Joint Arthroplasty: A Prospective Randomized Trial

University of Miami1 个研究点 分布在 1 个国家目标入组 2,396 人2025年2月1日

概览

阶段
不适用
干预措施
General Anesthesia
疾病 / 适应症
Knee Osteoarthritis
发起方
University of Miami
入组人数
2396
试验地点
1
主要终点
Length of hospital stay
状态
招募中
最后更新
上个月

概览

简要总结

The purpose of this research is to compare post-operative outcomes from patients undergoing TJA. The study team wants to learn about outcomes like length of hospital stay, post-operative pain scores, post-operative nausea, deep and superficial surgical site infection, periprosthetic fracture (a broken bone that occurs around an orthopaedic implant), implant dislocation, readmission rates, and revision rates.

注册库
clinicaltrials.gov
开始日期
2025年2月1日
结束日期
2030年3月1日
最后更新
上个月
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Principal Investigator
主要研究者

Victor Hugo Hernandez

Professor of Clinical

University of Miami

入排标准

入选标准

  • Patients undergoing a primary total hip or knee arthroplasty
  • Subjects must be capable of providing informed consent
  • English or Spanish speaking

排除标准

  • Patients with contraindications for spinal anesthesia such as:
  • Prior lumbar surgery with hardware insertion
  • Elevated intracranial pressure
  • Infection at the site of the procedure
  • Thrombocytopenia or coagulopathy
  • Severe mitral and aortic stenosis and left ventricular outflow obstruction
  • Severe spine pathology (spinal stenosis, spondylolisthesis, spondylosis) with radiculopathy and/or neurogenic claudication
  • Preexisting neurological disease
  • Patients with contraindications for general anesthesia such as:
  • Congestive heart failure

研究组 & 干预措施

General Anesthesia

Participants in this group will receive general anesthesia for TJA for up to 2 hours.

干预措施: General Anesthesia

Spinal Anesthesia

Participants in this group will receive spinal anesthesia for TJA for up to 2 hours.

干预措施: Spinal Anesthesia

结局指标

主要结局

Length of hospital stay

时间窗: Up to 72 hours.

Will be measured in hours.

Change in Patient Pain Scores as measured by the Numeric Rating Pain Scale

时间窗: Baseline (up to 1 hour after surgery), up to 24 hours.

Score range from 0 to 10, higher score indicate higher pain scores.

Change in Patient Nausea Scores as measured by the Conditioning Scoring Criteria

时间窗: Baseline (up to 1 hour after surgery), up to 24 hours.

Score range from 0 to 9, higher score indicate higher nausea scores.

Number of implant dislocation.

时间窗: Up to 90 days.

Will be measured by the number of implant dislocation.

Prosthetic joint infection

时间窗: Up to 90 days.

Will be measured by the 2018 Musculoskeletal Infection Society criteria.

Superficial surgical site infection

时间窗: Up to 90 days.

Will be measured by the 2018 Musculoskeletal Infection Society criteria.

Number of periprosthetic fracture

时间窗: Up to 90 days.

Will be measured by the number of periprosthetic fracture.

Number of participants who are readmitted 90 days after surgery.

时间窗: Up to 90 days.

Will be measured by the number of participants who are readmitted 90 days after surgery.

Number of participants who receive revision surgery 90 days after surgery.

时间窗: Up to 90 days.

Will be measured by the number of participants who receive revision surgery 90 days after surgery.

Number of participant deaths.

时间窗: Up to 90 days.

Will be measured by the number of participants deaths.

次要结局

  • Length of surgery.(Up to 2 hours.)

研究点 (1)

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