Şehit Prof. Dr. İlhan Varank Sancaktepe Training and Research Hospital
Istanbul, Sancaktepe, 34785, Turkey (Türkiye)
NCT Number: NCT07639762
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.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Istanbul, Sancaktepe, 34785, Turkey (Türkiye)
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
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
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.
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.
Time frame: From the end of surgery to 48 hours
Postoperative complications will be recorded during the postoperative follow-up period.
Time frame: Perioperative/Periprocedural
Time to first mobilization will be recorded as the time from the end of surgery to the first postoperative mobilization.
Time frame: Perioperative/Periprocedural
Length of hospital stay will be recorded as the time from surgery to hospital discharge.
Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
Other
Kalça kırıklarında Ultrason rehberliğinde yapılan Supra-inguinal Fasya Iliaca ve Lomber Erektor Spina Plan bloğunun Etkinliklerinin karşılaştırılması
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.
Published trials that share one or more normalized conditions with this study.
NCT06989047
Agnosia, Femoral Fractures
View Trial DetailsNCT07597317
Femoral Fractures, Femoral Nerve
Lahore, Punjab Province, Pakistan
View Trial DetailsNCT04285333
Acute Pain, Agnosia
Tunis, Tunisia
View Trial DetailsNCT04692428
Agnosia, Femoral Fractures
Nabeul, Mrezga, Tunisia
View Trial Details