tilization, Availability of Analgesics and Quality of Pain Control for Post-operative Pain in Surgical Patients

Not Applicable

Completed

• Conditions: Post- operative pain; analgesics; post- drug utilization

• Registration Number: TCTR20180808006
• Lead Sponsor: Self

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2016-08-31
• Study Start: 2018-08-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 233

Inclusion Criteria

- both male and female patients of age ≥ 13 yrs
- patients underwent elective major operations which used spinal, general anesthesia or epidural anesthesia
- patients who give informed consent

Exclusion Criteria

- patients who are seriously ill
- patients with mental disorder
- patients unable to respond to verbal questions
- operation under local anesthesia

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
tilization of analgesics 24 hour post-operative period Number and percentage,Drug Utilization 90% 24 hour post-operative period Drugs in DU 90% segment,Defined daily dose (DDD) 24 hour post-operative period DDD/1000 inhabitants/day

Secondary Outcome Measures

Name	Time	Method
Quality of pain control 24 hour post-operative period Pain Management Index (PMI) and Numerical rating scale (NRS)