Comparison of median and Para median methods in the incidence of Post-Dural-puncture headache in patients undergoing Orthopedic Lower Limb Surgery by spinal anesthesia

Not Applicable

• Conditions: Orthopedic patients.; Fracture of bone following insertion of orthopedic implant, joint prosthesis, or bone plate; M96.6

• Registration Number: IRCT20210415050976N3
• Lead Sponsor: Jahrom University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 June 2021

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

People who will be operated with spinal anesthesia.
Hemodynamic stability

Exclusion Criteria

Chronic pain and cancer
Anxiety and mental illness
Infection at the site of needle entry
Coagulation disorders

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Headache. Timepoint: Up to 7 days after surgery. Method of measurement: Post-Dural-puncture headache criteria.

Secondary Outcome Measures

Name	Time	Method
Vital signs. Timepoint: Before spinal anesthesia, after spinal anesthesia and at 5, 15 and 30, 45, 60 and 90 minutes during surgery and in recovery. Method of measurement: Monitoring device.