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Clinical Trials in Turkey / NCT07346885
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Lumbar-Sacral Plexus Block vs Fascia Iliaca Block Plus Low-Dose Spinal Anesthesia for Femoral Neck Fracture Surgery

NCT07346885 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-12-30
Last updated
2026-01-16

Condition(s) studied

Femoral Neck FracturesNerve Block

Investigational drug(s) / intervention(s)

Lumbar and Sacral Plexus BlockFascia Iliaca Block Combined with Low-Dose Spinal Anesthesia

Lumbar and Sacral Plexus Block: For lumbar and sacral plexus blocks, a 10-15 cm ultrasound-visible peripheral nerve block needle and a nerve stimulator will be used. For lumbar plexus shamrock imaging and sacral plexus blocks, parasacral imaging will be used. 0.5% bupivacaine will be used as the local anesthetic.

Fascia Iliaca Block Combined with Low-Dose Spinal Anesthesia: Spinal anesthesia will be administered using a 25-gauge Quincke needle. After positioning the patient on the side to be operated on in a lateral position, hypobaric spinal anesthesia will be administered through an appropriate (L3-4 or L4-5) with 1.5 cc of local anesthetic mixture. Before receiving spinal anesthesia, patients will undergo a supra-inguinal fascia iliaca block with 20 to 30 milliliters of 0.25% local anesthetic (bupivacaine).

Study summary

Femoral neck fracture surgery in elderly patients is frequently complicated by intraoperative hypotension and inadequate postoperative analgesia. Regional anesthesia techniques are increasingly preferred to reduce hemodynamic instability and improve pain control. This prospective observational study aims to compare the efficacy of lumbar and sacral plexus block with fascia iliaca block combined with low-dose spinal anesthesia in terms of severe intraoperative hypotension and postoperative analgesic outcomes in patients undergoing surgery for femoral neck fracture.

Eligibility

Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: -\>18 years and \<90 years * American Society of Anesthesiologists score between I and IV * Patients who will undergo femoral neck fracture surgery Exclusion Criteria: * Previous local anesthetic allergy * Those with bleeding diathesis disorder * Having a mental disorder * Those who are allergic to the drugs used * Patients who did not consent to participate in the study * Presence of infection in the block area * Body mass index \>30 * Preoperative or intraoperative general anesthesia * Patients for whom consent cannot be obtained * Pregnant patients

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Health Sciences,,Bursa Yuksek Ihtisas Training and Research Hospital, Bursa Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07346885 on ClinicalTrials.gov ↗ ← All trials in Turkey