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Effect of Anesthesia Technique on Outcome After Hip Fracture Surgery in Elderly Adult Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02458547
Enrollment
186
Registered
2015-06-01
Start date
2015-05-31
Completion date
2019-01-21
Last updated
2019-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Fracture

Brief summary

Despite many previous studies, whether anesthetic technique will significantly affect overall patient outcome, morbidity and mortality in elderly hip fracture patients is controversial. Due to old age, poor patient condition and emergent clinical settings, patients undergoing surgical procedures for hip fracture management are often subject to poor postoperative outcome and high mortality rates. While many studies have reported that regional anesthesia leads to improved postoperative outcome after hip fracture surgery, others have concluded otherwise. Moreover, because the majority of these previous studies are retrospective cohorts or systemic reviews, there is a need for randomized clinical trials to provide high quality evidence. This study aims to compare patient outcome between three different anesthetic techniques in elderly patients undergoing surgery for hip fracture management by evaluating proinflammatory cytokines, chemistry lab testing and clinical outcome between general anesthesia with either desflurane or propofol-based TIVA and spinal anesthesia with bupivacaine.

Interventions

DRUGDesflurane

Inhalation anesthesia with desflurane at age-adjusted MAC of 0.8\ 1.0

DRUGPropofol

Total intravenous anesthesia with propofol target controlled infusion

DRUGBupivacaine

Spinal anesthesia with 0.5% bupivacaine

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1\. Patients older than 65 years scheduled for elective or emergency hip fracture surgery.

Exclusion criteria

1. Patient refusal 2. Inflammation or wound at puncture site, increased intracranial pressure, bleeding diathesis 3. Allergies to propofol or its ingredients, soybeans or peanuts 4. Patients with altered mental status 5. Illiterate patients or foreigners

Design outcomes

Primary

MeasureTime frame
HMGB1from preoperative baseline to 72hours
IL-6from preoperative baseline to 72hours
NT-proBNPfrom preoperative baseline to 72hours
hemoglobinfrom preoperative baseline to 72hours
total lymphocyte countfrom preoperative baseline to 72hours
albuminfrom preoperative baseline to 72hours
creatininefrom preoperative baseline to 72hours
potassiumfrom preoperative baseline to 72hours
troponin-Tfrom preoperative baseline to 72hours
CRPfrom preoperative baseline to 72hours

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026