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Clinical Trials/NCT01681238
NCT01681238
Unknown
Not Applicable

A Randomized Study of Goal-directed Therapy in the Elderly High-risk Patients Undergoing Total Hip Replacement

Guangzhou First People's Hospital1 site in 1 country72 target enrollmentSeptember 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Perioperative/Postoperative Complications
Sponsor
Guangzhou First People's Hospital
Enrollment
72
Locations
1
Primary Endpoint
length of postoperative hospital stay
Last Updated
13 years ago

Overview

Brief Summary

There is growing evidence that the risk of postoperative complications can be decreased by optimizing the amount and type of infusion fluids given during surgery, steered by goal-directed therapy based on flow-related hemodynamic parameters, particularly in high-risk patients. This study is undertaken subsequently to test the hypothesis that the intraoperative goal-directed strategy based on FloTrac/Vigileo, a minimally invasive monitor, can partially prevented postoperative complications and shorten hospital stay in the elderly high-risk patients undergoing total hip replacement with continuous spinal anaesthesia .

Detailed Description

After sedated with IV 0.02 mg/kg midazolam, all patients will receive arterial, central venous, and L3-4 intrathecal catheterizations. A T12 sensory level block was attained with ropivacaine through the intrathecal catheter. Besides currently recommended monitoring during the intraoperative period, arterial blood pressure, stroke volume (Edwards Lifesciences, Irvine, Calif.), and central venous oxygen saturation (Edwards Lifesciences) will be measured and recorded. All Patients will receive intranasal oxygen 2 mL/min and be kept normothermic (body temperature \> 36°C). Patients in both groups receive 8 mL/kg/hour of Ringer's lactate solution from 30 minutes prior to induction of anaesthesia through the end of surgery, when the rate will be decreased to 100 mL/hour. In addition, boluses of colloid will be given to different protocol group according to the study arm to which the patient allocated.Postoperative care and discharge criteria were predefined using the hospital care map and protocol.

Registry
clinicaltrials.gov
Start Date
September 2012
End Date
June 2013
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Guangzhou First People's Hospital
Responsible Party
Principal Investigator
Principal Investigator

Xiangcai Ruan

Professor, Vice Chair

Guangzhou First People's Hospital

Eligibility Criteria

Inclusion Criteria

  • Adult patients scheduled for total hip replacement at this institution.
  • American Society of Anaesthesiologists (ASA) physical status of III or VI.
  • Two or more risk factors according to risk index of Lee .

Exclusion Criteria

  • Age under 70years old
  • idiopathic coagulopathy: with warfarin or heparin
  • systemic or local infection
  • unable to cooperate
  • spinal trauma or severe low back pain history
  • patient refusal.

Outcomes

Primary Outcomes

length of postoperative hospital stay

Time Frame: 28 days

days from end of surgery to hospital discharge.

Secondary Outcomes

  • postoperative complications and mortality(28 days)

Study Sites (1)

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