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Comparison of Pericapsular Nerve Group Block With Suprainguinal Fascia Compartment Block in Hip Fractures

Completed
Conditions
Hip Fractures
Interventions
Procedure: PENG block+ SIFCB
Procedure: PENG block
Registration Number
NCT06169462
Lead Sponsor
Karaman Training and Research Hospital
Brief Summary

Ultrasound-guided Supra-inguinal Fascia Iliaca compartment Block (SIFCB) and Pericapsular Nerve Group Block (PENG) are increasingly being used for postoperative analgesia for hip surgery. The postoperative analgesic efficacy of SIFCB added to PENG block in elderly hip fracture patients will be evaluated. Postoperative opioid consumption and quality of recovery will also be evaluated.

Detailed Description

The study was conducted as a retrospective cohort feasibility design within a tertiary hospital. Patient records and electronic data systems were used to gather the required data for analysis. Before surgery, a carefully selected cohort of patients who underwent PENG block and PENG block added SIFCB were included in the study.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
38
Inclusion Criteria
  • Physical status according to American Society of Anesthesiologists (ASA ) I-III
Exclusion Criteria
  • Previous operation on the same hip
  • Hepatic or renal insufficiency
  • Patients undergoing general anesthesia
  • Allergy or intolerance to one of the study medications
  • BMI >40
  • ASA IV

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Suprainguinal fascia compartment block (SIFCB) + PENGPENG block+ SIFCBPatients who underwent PENG+SIFCB in Hip surgery under spinal anesthesia will be evaluated retrospectively in terms of opioid consumption and NRS scores.
Pericapsular nerve group (PENG) blockPENG blockPatients who underwent PENG in Hip surgery under spinal anesthesia will be evaluated retrospectively in terms of opioid consumption and NRS scores.
Primary Outcome Measures
NameTimeMethod
Opioid consumptionPostoperative 48th hour

If the patient's Numerical Rating Scale (NRS) score is equal to or above 4, tramadol 50 mg IV or oxycodone 5 mg orally every 4 hours will be administered as rescue analgesia.

Secondary Outcome Measures
NameTimeMethod
Postoperative complications24 hours

Presence of postoperative nausea, vomiting, pruritus, urinary retention, respiratory depression

Numerical Rating Scale (NRS) scoresPostoperative 48th hour

Range 0-10, 0=no pain, 10=the worse pain ever

Quality of Recovery 15 ScorePostoperative day 1 and 1 month

Quality of Recovery (QoR)-15 survey.Minimum value: 0, Maximum value: 150, higher scores mean better

Mobilization time24 hours

Mobilization time

Trial Locations

Locations (1)

Karaman Training and Research Hospital

🇹🇷

Karaman, Karaman/Merkez, Turkey

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