Comparing Suprainguinal Fascia Iliaca Block With Erector Spinae Plane Block in Hip and Proximal Femur Surgery

Postoperative Pain Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05642975
• Other study ID #: 11.2022.546
• Status: Completed
• Start date: August 1, 2022
• Est. completion date: May 1, 2023

Study information

• Verified date: October 2023
• Source: Marmara University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 63
• Est. completion date: May 1, 2023
• Est. primary completion date: May 1, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

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.

Related Conditions & MeSH terms

• Femoral Fractures
• Femur Fracture
• Pain, Postoperative
• Postoperative Pain
• Regional Anesthesia

Intervention

Procedure:
• Regional Block Comparison
Comparing postoperative pain and opioid consumption in groups

Locations

Country	Name	City	State
Turkey	Marmara University Hospital	Istanbul

Sponsors (1)

Lead Sponsor	Collaborator
Marmara University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Postoperative Pain Scores	Comparing pain scores with Numeric Rating Scale (NRS)	48 hours
Primary	Opioid Consumption	Comparing opioid consumption via Patient Controlled Analgesia (PCA) device	48 hours
Secondary	Patient Satisfaction	patient satisfaction score: 0: unsatisfied 5: fully satisfied	48 hours
Secondary	Complications Related to Pain Management	complications such as hypothension, nausea, vomiting, itching	48 hours
Secondary	Time of Mobilisation	time frame between the surgery to first mobilization (walking)	7 days