Comparison of different volumes of local anesthetic used for fascia iliaca compartment block

Phase 4

Completed

• Conditions: Post-operative pain; Femur disorder requiring surgery; Knee disorder requiring surgery; Anaesthesiology - Pain management; Musculoskeletal - Other muscular and skeletal disorders

• Registration Number: ACTRN12616000892415
• Lead Sponsor: metin KILINC

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-07-06
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

Studies elective knee or femur surgery operations to be done with ASA I-II-III patients between the ages of 18 -80 will be included

Exclusion Criteria

ASA IV-V
studies did not approve those,
abnormal coagulation profile Those with neurologic deficits to be implemented drug history of allergy sufferers,
pregnant women, dermatological disorders, and those with psychiatric patients suffering from the study will be kept

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
postoperative pain will be assessed by 100mm(10 cm) visual analogue scale, [in first 24 hours after completion of block. (0, 1, 2, 4, 6, 12, 24th hour after fascia iliaca compartment block).]

Secondary Outcome Measures

Name	Time	Method
to evaluate additional analgesic need. cumulative diclofenac sodium doses will be recorded[in first 24 hours after completion of block. (0, 1, 2, 4, 6, 12, 24th hour after fascia iliaca compartment block).]