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临床试验/NCT02230657
NCT02230657已完成不适用

A Prospective, Randomized Trial Comparing Same Day Discharge and Overnight Hospital Stay Among Total Hip Arthroplasties Done by the Direct Anterior Approach

Rothman Institute Orthopaedics4 个研究点 分布在 1 个国家开始时间: 2014年9月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
试验地点
4
主要终点
Patient Satisfaction

研究概览

简要总结

The purpose of this study is to identify differences in satisfaction, pain and length of stay between patients undergoing hip replacement who are discharged from the hospital on the day of surgery compared to patients who stay one night in the hospital.

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Primary THA without acute hip fracture or prior hardware that would need to be removed at the time of surgery
  • Unilateral THA
  • Pre-operative Body Mass Index (BMI) < 40 kg/m2
  • Age < 75 years at time of surgery
  • Pre-operative hemoglobin > 10 g/dL if pre-operative hemoglobin data is available
  • No history of cardiopulmonary disease that would necessitate inpatient monitoring after surgery
  • Pre-operative ambulatory status does not require the use of a walker or wheelchair
  • No chronic pre-operative opioid medication use or opioid addiction
  • Assistance available at home after discharge from hospital
  • No other condition or circumstance that would preclude rapid discharge from the hospital after surgery
  • Subject's English proficiency allows understanding of study and Informed Consent
  • Subject consented to participate in this study

排除标准

  • Revision THA
  • Bilateral THA
  • Pre-operative BMI ≥ 40 kg/m2
  • Age ≥ 75 at time of surgery
  • Pre-operative hemoglobin ≤ 10 g/dL if pre-operative hemoglobin data is available
  • History of cardiopulmonary disease requiring acute inpatient monitoring
  • Pre-operative ambulatory status requiring the use of a walker or wheelchair
  • Chronic pre-operative opioid medication use or opioid addiction
  • Limited or no assistance available at home after discharge from hospital
  • Any other condition or circumstance that would preclude rapid discharge from the hospital
  • Subject not proficient in English
  • Subject did not consent to participate in this study

结局指标

主要结局

Patient Satisfaction

时间窗: Discharge through 30 days post-op

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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