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Comparison of Sacral Erector Spinae Plane Block and Supra-Inguinal Fascia Iliaca Block for Analgesia After Hip Fracture Surgery

Comparison of Postoperative Analgesic Efficacy of Preoperatively Performed Sacral Erector Spinae Plane Block and Supra-Inguinal Fascia Iliaca Block in Patients Undergoing Surgery for Hip Fracture

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07081867
Enrollment
77
Registered
2025-07-23
Start date
2025-01-15
Completion date
2025-12-01
Last updated
2026-01-23

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

Conditions

Elderly Patients, Hip Fracture Surgery, Postoperative Pain Management, Regional Anesthesia

Keywords

Nerve Block, Anesthesia, Regional, Hip Fractures, Postoperative Pain, Analgesia, Visual Analog Scale, Pain Measurement

Brief summary

This study compares the postoperative analgesic effectiveness of Sacral Erector Spinae Plane Block (SESPB) and Supra-Inguinal Fascia Iliaca Block (SIFIB) in patients undergoing hip fracture surgery. Both techniques are regional anesthesia methods aiming to reduce postoperative pain and opioid consumption. The study evaluates pain scores, opioid requirements, mobilization times, and hospital discharge times to determine which block provides more effective pain management in different postoperative periods.

Detailed description

Hip fractures are common injuries among elderly patients, often resulting in high rates of morbidity and mortality. Effective postoperative pain management plays a critical role in reducing complications such as delayed mobilization, deep vein thrombosis, pneumonia, and prolonged hospitalization. Regional anesthesia techniques, including Sacral Erector Spinae Plane Block (SESPB) and Supra-Inguinal Fascia Iliaca Block (SIFIB), have gained popularity as part of multimodal analgesia strategies that aim to minimize opioid use and improve postoperative comfort. However, there is limited evidence comparing these two techniques directly. In this prospective observational study, patients aged 65 and older undergoing hip fracture surgery under spinal anesthesia were included. After obtaining informed consent, patients received either SESPB or SIFIB for postoperative analgesia in addition to the standard anesthetic protocol. Pain levels were assessed using the Visual Analog Scale (VAS) at 1, 6, 12, and 24 hours after surgery. Additional data such as total opioid consumption within 24 hours, time to first analgesic requirement, mobilization time, and length of hospital stay were recorded. The results demonstrated that patients who received SIFIB had significantly lower pain scores in the early postoperative period (1st hour), while patients who received SESPB experienced better pain relief in the late postoperative period (24th hour). No significant differences were observed between the groups in terms of total opioid consumption, mobilization time, or hospital stay duration. No complications related to the block procedures were reported. This study suggests that both SESPB and SIFIB are safe and effective regional anesthesia techniques for postoperative pain management in hip fracture surgeries. The selection between these blocks may be based on the desired onset and duration of analgesia, with SIFIB providing superior early pain control and SESPB offering more prolonged analgesic effects.

Interventions

PROCEDURESupra-inguinal Fascia Iliaca Block (SIFIB)

Ultrasound-guided injection of 40 mL of 0.25% bupivacaine between the iliacus muscle and fascia iliaca via a supra-inguinal approach, performed preoperatively for postoperative analgesia in patients undergoing hip fracture surgery under spinal anesthesia.

PROCEDURESacral Erector Spinae Plane Block (SESPB)

Ultrasound-guided injection of 40 mL of 0.25% bupivacaine into the fascial plane deep to the erector spinae muscle at the sacral level (S2), performed preoperatively for postoperative analgesia in patients undergoing hip fracture surgery under spinal anesthesia.

Sponsors

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patients aged 65 years and older * Patients undergoing surgery for hip fractures under spinal anesthesia * Patients who are oriented and cooperative * Patients who have signed an informed consent form

Exclusion criteria

* Patients with contraindications for spinal anesthesia * Patients with Alzheimer's disease or dementia, and those who are non-oriented or non-cooperative * Patients with major organ failure (such as heart, liver, or kidney failure) * Patients who decline to participate in the study * Patients classified as American Society of Anesthesiologists (ASA) Physical Status IV or higher * Patients with pathological fractures or bone metastasis

Design outcomes

Primary

MeasureTime frameDescription
Postoperative Pain ScoresAt 1 hour, 6 hours, 12 hours, and 24 hours postoperatively.Pain intensity measured using the Visual Analog Scale (VAS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst pain imaginable. Pain scores will be recorded at specific postoperative time points: 1st, 6th, 12th, and 24th hours.
Time to First Postoperative Analgesic RequirementUp to 48 hours postoperatively.Time interval from end of surgery to the first request for analgesia.
Total Postoperative Opioid ConsumptionA weekThe total amount of opioids required by patients during the postoperative period.
Time to First MobilizationFrom the end of surgery until first mobilization, typically within 24 to 48 hours postoperativelyThe time until patients' first mobilization (walking or standing) after surgery.

Secondary

MeasureTime frameDescription
Length of Hospital StayUp to 14 days postoperatively.Duration from the day of surgery to the day of hospital discharge, measured in calendar days.
Block-Related ComplicationsA weekPossible complications following Sacral Erector Spinae Plane Block (SESPB) and Supra-Inguinal Fascia Iliaca Block (SIFIB), such as nerve injury, infection, hematoma, etc.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORBeyzanur Aydogdu

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Outcome results

None listed

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