Effects of patient education on pain managment

Not Applicable

Recruiting

Conditions: Condition 1: Fracture of spine, level unspecified. Condition 2: Fracture of lumbar spine and pelvis.
Fracture of spine, level unspecified
Fracture of lumbar spine and pelvis

Registration Number: IRCT20170123032129N5

Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 60

Inclusion Criteria

Patients who have elective Spinal culumn surgery
All patients who have the ability to communicate verbally
All patients who have been hospitalized at least one night before surgery
All patients do not have a history of substance abuse and Opioid drug addiction
Participants do not have a history of using patient-controlled analgesia pump
All patients who have received general anesthesia

Exclusion Criteria

Patients who have emergency Spinal culumn surgery
All patients have a history of substance abuse and Opioid drug addiction
All patients who have allergic reactions to any components of analgesia pump
All patients who are receiving analgesic agent other than pain control pump

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain severity. Timepoint: 2, 4 and 24 after surgery. Method of measurement: Numerical rating scale.

Secondary Outcome Measures

Name	Time	Method
Pain control quality. Timepoint: 24 hours after surgery. Method of measurement: APS-POQ-R(American Pain Society Patient Outcome Questionnaire ).;Severity of nausea. Timepoint: 2,4 and 24 hours after surgery. Method of measurement: VAS(visual analog scale).;Times of nausea. Timepoint: 2,4 and 24 hours after surgery. Method of measurement: subjective.;Times of vomiting. Timepoint: 2,4 and 24 hours after surgery. Method of measurement: visual.;Blood pressure. Timepoint: 2,4 and 24 hours after surgery. Method of measurement: sphygmomanometer.;Sedation. Timepoint: 2,4 and 24 hours after surgery. Method of measurement: Ramsy scale.;Drug dose used. Timepoint: 24 hours after surgery. Method of measurement: measurement of drug residual dose.;Awareness of patients about PCA. Timepoint: 2,4 and 24 hours after surgery. Method of measurement: A questionnaire with 7 questions about patient awareness about the PCA pump.