Regional Anesthesia for Lower Extremity Surgery

Completed

• Conditions: Erector Spinae Plane Block; Sciatic Nerve Block; Lower Extremity Surgery

• Registration Number: NCT06777953
• Lead Sponsor: Haseki Training and Research Hospital

Brief Summary

In this study, patients who underwent osteosynthesis with plate via standard anterolateral incision due to proximal tibia fracture in the orthopedic clinic within the last year; those who underwent perioperative anesthesia with spinal block, those who underwent postoperative analgesia with Ultrasound-guided popliteal sciatic nerve block, lumbar-sacral Erector Spine plane block combinations in the recovery unit will be identified and their files will be scanned retrospectively. Gender, surgical duration, postoperative block, pre-post block pain levels will be reviewed via Visual Analog Scale scoring, postoperative analgesics consumed and their amounts, Bromage scale, mobilization times, block-related complications, satisfaction levels will be determined and these two groups of patients who underwent block will be compared in terms of analgesia, complications, and satisfaction.

Detailed Description

Not available

Study Timeline

• Study Start: 2024-11-01
• Primary Completion: 2024-12-15
• Study Completion: 2024-12-28
• Status Verified: 2025-01
• Study First Submitted: 2025-01-04
• Study First Submitted QC: 2025-01-10
• Last Update Submitted: 2025-01-10
• Study First Posted: 2025-01-16
• Last Update Posted: 2025-01-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 32

Inclusion Criteria

• Patients aged 18-65
• Patients undergoing spinal anesthesia
• Patients undergoing postoperative erector spinae plane block
• Patients undergoing postoperative sciatic nerve block

Exclusion Criteria

• Pregnant patients
• Patients who cannot be contacted
• Patients who have undergone perioperative general anesthesia
• Patients with a history of cerebrovascular disease
• Patients with data loss
• Patients who did not receive consent

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative Analgesia	24 hours	Postoperative analgesia will be assessed by Visual Analog Scale Score and postoperative analgesic consumption. The visual analog scale is a numerical assessment ranging from 0 to 10. A score of 0 is considered as no pain, a score of 5 is considered as moderate pain, and a score of 10 is considered as unbearable pain. Rescue intravenous analgesic treatment is applied to scores of 4 and above.

Secondary Outcome Measures

Name	Time	Method
Block related complication	24 hours	Patients will be evaluated with Bromage Scale and mobilization times.The bromage scale is a numerical assessment ranging from 0 to 3. A score of 0 is No motor block, a score of 1 is Inability to raise extended leg; able to move knees and feet no pain, a score of 2 is Inability to raise extended leg and move knee; able to move feet, a score of 3 is Complete block of motor limb.It will also be checked when the patients can walk after the motor block has passed.

Trial Locations

Locations (1)

Haseki Training and Research Hospital; 🇹🇷 Istanbul, Turkey