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

Comparison of Pericapsular Nerve Group (PENG) Block Alone Versus Combined With Suprainguinal Fascia Compartment Block (SIFCB) for Postoperative Analgesia and Quality of Recovery in Older Adult Patients With Hip Fractures

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06169462
Enrollment
38
Registered
2023-12-13
Start date
2023-01-31
Completion date
2023-12-10
Last updated
2023-12-14

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

Conditions

Hip Fractures

Keywords

Anesthesia, Lower extremity, pericapsular nerve group block, suprainguinal fascia compartment block

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.

Interventions

PROCEDUREPENG block

Patients underwent ultrasound-guided PENG Block for older adult patients surgery for hip fracture. Patients who received opioids as a rescue analgesic during postoperative pain management on selected dates will be included in the study.

PROCEDUREPENG block+ SIFCB

Patients underwent ultrasound-guided PENG Block+ SIFCB for older adult patients surgery for hip fracture. Patients who received opioids as a rescue analgesic during postoperative pain management on selected dates will be included in the study.

Sponsors

Karaman Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to 90 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Opioid consumptionPostoperative 48th hourIf 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

MeasureTime frameDescription
Numerical Rating Scale (NRS) scoresPostoperative 48th hourRange 0-10, 0=no pain, 10=the worse pain ever
Quality of Recovery 15 ScorePostoperative day 1 and 1 monthQuality of Recovery (QoR)-15 survey.Minimum value: 0, Maximum value: 150, higher scores mean better
Postoperative complications24 hoursPresence of postoperative nausea, vomiting, pruritus, urinary retention, respiratory depression
Mobilization time24 hoursMobilization time

Countries

Turkey (Türkiye)

Outcome results

None listed

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