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Completed

NCT Number: NCT07639762

Comparison of the Efficacy of Ultrasound-guided Supra-inguinal Fascia Iliaca and Lumbar Erector Spina Plan Block in Hip Fractures

The aim of our study was to evaluate the efficacy and patient satisfaction level of SI-FIB and lumbar ESPB for positioning and postoperative analgesia during spinal anesthesia in patients undergoing hip fracture surgery.

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Key information

About this study

Hip fractures, which are one of the leading causes of mortality and morbidity with increasing age, are common and usually require surgery and cause severe pain in the perioperative period, which may result in delirium, sleep disturbances and chronic pain. This pain can be managed using neuraxial and regional techniques, as well as pharmacologic agents such as nonsteroidal analgesics, opioids and gabapentinoids, and interventions such as periarticular injections and peripheral nerve blocks. Supra-inguinal fascia iliaca block (SI-FIB) is a technique that blocks all components of the lumbar plexus, including the femoral nerve, latero-femoral nerve and obturator nerve. It is thought to function in a similar way to the anterior lumbar plexus block. Studies have successfully demonstrated the effectiveness of SIFIB in reducing postoperative pain after hip surgery. The lumbar erector spina plan block (ESPB) has been described for use in hip and femur surgery and radiologic evaluation and clinical results have shown that it provides similar analgesia to the lumbar plexus block at high volumes. It is accepted that multimodal analgesia is the best option for pain control and peripheral nerve blocks are effectively applied for this purpose. In this way, opioid use and related side effects such as nausea, vomiting, pruritus and sedation are reduced, and early mobilization, reduced hospital stay and prevention of postoperative complications are also contributed.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years of age or older
  • American Society of Anesthesiologists (ASA) I-III risk class,
  • Patients and/or guardians informed and given informed consent regarding the study

Exclusion criteria

  • Central-autonomic nervous system or neuropsychiatric disorders,
  • Opioid use,
  • Contraindications for the planned block,
  • Known allergies to the medications to be administered,
  • Patients who refuse to participate in the study

Treatment and study plan

Primary outcomes

  1. Assessment of pain during spinal anesthesia position

    Time frame: The NRS score will be recorded before the block. The NRS score will be recorded 20 minutes after the block is administered. The NRS score will be recorded when the patient is placed in a sitting position for spinal anesthesia.

    The primary objective of our study is to compare the effectiveness of SI-FIB and lumbar ESPB in patients undergoing hip fracture surgery by evaluating NRS scores during positioning for spinal anesthesia.

Secondary outcomes

  1. Postoperative Pain Intensity at Rest and During Activity

    Time frame: 0, 2, 6, 12, and 24 hours postoperatively

    Postoperative pain intensity at rest and during activity will be assessed using the Numeric Rating Scale. The Numeric Rating Scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate worse pain.

    Unit of Measure: Numeric Rating Scale score

  2. Additional Analgesic Consumption

    Time frame: From the end of surgery to 24 hours postoperatively

    Additional analgesic consumption will be recorded as the total amount of rescue analgesic administered postoperatively.

  3. Patient Satisfaction With Postoperative Analgesia

    Time frame: 24 hours postoperatively

    Patient satisfaction with postoperative analgesia will be assessed using a 4-point satisfaction scale. The scale ranges from 1 to 4, where 1 indicates very satisfied, 2 indicates satisfied, 3 indicates undecided, and 4 indicates not satisfied. Higher scores indicate lower satisfaction.

Other outcomes

  1. Postoperative Complications

    Time frame: From the end of surgery to 48 hours

    Postoperative complications will be recorded during the postoperative follow-up period.

  2. Time to First Mobilization

    Time frame: Perioperative/Periprocedural

    Time to first mobilization will be recorded as the time from the end of surgery to the first postoperative mobilization.

  3. Length of Hospital Stay

    Time frame: Perioperative/Periprocedural

    Length of hospital stay will be recorded as the time from surgery to hospital discharge.

Sponsors and collaborators

Lead sponsor

Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital

Other

Registry information

Official study title

Kalça kırıklarında Ultrason rehberliğinde yapılan Supra-inguinal Fasya Iliaca ve Lomber Erektor Spina Plan bloğunun Etkinliklerinin karşılaştırılması

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 10, 2026
Registry last updated
Jun 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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