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Clinical Trials/NCT05642975
NCT05642975
Completed
Not Applicable

Comparing Ultrasound-Guided Suprainguinal Fascia Iliaca Block With Lumbar Erector Spinae Plane Block in Hip and Proximal Femur Fracture Surgery

Marmara University1 site in 1 country66 target enrollmentAugust 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Marmara University
Enrollment
66
Locations
1
Primary Endpoint
Opioid Consumption
Status
Completed
Last Updated
last year

Overview

Brief Summary

Most hip fractures occur in the elderly population. Opioid-related respiratory depression is more common in the elderly population but can cause severe brain damage or death. Reducing the amount of opioids administered before, during and after surgery by adding a regional block may increase the postoperative quality of recovery, reduce chronic pain syndromes, and may potentially facilitate the participation of patients in rehabilitation.

Despite their potential advantages, peripheral nerve blocks are still not widely used in people with hip fractures.

The primary objective of this study is to compare patients' postoperative pain scores and opioid consumption.

Registry
clinicaltrials.gov
Start Date
August 1, 2022
End Date
May 1, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients over 18 years old, undergoing hip fracture surgery

Exclusion Criteria

  • Patients with solid organ dysfunction, chronic opioid or corticosteroid use, bleeding diathesis, patients receiving inpatient medication, patients with psychiatric disorders and patients who cannot be contacted after surgery.

Outcomes

Primary Outcomes

Opioid Consumption

Time Frame: 48 hours

Comparing opioid consumption via Patient Controlled Analgesia (PCA) device

Secondary Outcomes

  • Patient Satisfaction(48 hours)
  • The lengths of ICU and hospital stays(7 days)
  • Complications Related to Pain Management(48 hours)
  • Postoperative Pain Scores(48 hours)

Study Sites (1)

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