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Dexmedetomidine vs Propofol Sedation Reduces Postoperative Delirium in Patients Receiving Hip Arthroplasty.

T

The First Affiliated Hospital of Anhui Medical University

Status

Completed

Conditions

Local Anesthesia
Anesthesia

Treatments

Drug: dexmedetomidine
Drug: propofol

Study type

Interventional

Funder types

Other

Identifiers

NCT02793986
PJ2015-07-12

Details and patient eligibility

About

With blocks of lumbar and lumbar plexus, we can reduce the intravenous anesthetics usage. To offer an satisfied surgery process for patients, a proper sedation is necessary. So in this study, we want to investigate the influence of two different sedative drugs on outcomes of patients received hip replacement surgery .

Enrollment

296 patients

Sex

All

Ages

65 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 65 years or older and undergoing hip fracture repair

Exclusion criteria

  • Patients with severe cognitive impairment (MMSE score, <15)
  • Preoperative delirium as determined by Confusion Assessment Method
  • Contraindications to local anesthesia
  • Prior hip surgery
  • Mental or language barriers that would preclude data collection
  • Severe congestive heart failure (NewYork Heart Association class IV)
  • Severe chronic obstructive pulmonary disease (Global Initiative for Chronic Obstructive Lung Disease guidelines, stage III-IV)

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

296 participants in 2 patient groups

dexmedetomidine sedation
Experimental group
Description:
Patients received local anesthesia, in this arm, the sedation of patients was achieved with a bolus of dexmedetomidine at 1.0 μg/kg (over a period of 15 to 20 min) and followed by an infusion of dexmedetomidine at 0.2-0.7 μg/kg/h.
Treatment:
Drug: dexmedetomidine
propofol sedation
Experimental group
Description:
Patients received local anesthesia, in this arm, the sedation of patients was achieved with a target-controlled infusion (TCI) of propofol, and the effect site concentration was set to 0.8-1.0μg/ml.
Treatment:
Drug: propofol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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