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Clinical Trials/NCT05624502
NCT05624502
Recruiting
Not Applicable

Mprovement in Postoperative Pain Outcome: Pain Registry

King Saud University1 site in 1 country1,000 target enrollmentJanuary 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Post Operative Pain
Sponsor
King Saud University
Enrollment
1000
Locations
1
Primary Endpoint
dynamic and static pain
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

This is an observational study project aims at improving postoperative pain outcomes by evaluating the current status of postoperative pain managements in the institution. Then the investigators will compare the results by internal and external benchmarking. Then they will suggest recommendations to improve the current situation of postoperative pain management.

Detailed Description

At least half of the patients suffer from moderate to severe post-operative pain. The price of poorly managed pain is high: pain impedes recovery, causes suffering and prolongs the hospital stay. PAIN OUT provides tools for measurement, feedback and benchmarking of pain treatment quality in order to improve patient care. A research project that aims at improving postoperative pain treatment outcomes by evaluating the current status of postoperative pain managements in our institution. Then the investigators compare the results by internal and external benchmarking. Then suggest recommendations to improve the current situation of postoperative pain management. parameters include" Patient's data Pain assessments by using the visual analogue score of 11 point (from "0" no pain - "10" worst pain) will be evaluated as the following: Worst pain since surgery, Least pain since surgery, Pain score at rest. Pain score during movements in bed, Pain score during deep breathing and coughing, How often the severe pain since surgery (%), Does the pain interfere with sleeping pattern, and the side effects.

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
December 31, 2024
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

SALAH EL-TALLAWY

Professor and Consultant - Anesthesia and Pain Management

King Saud University

Eligibility Criteria

Inclusion Criteria

  • Postoperative patients during the first 24 hours of surgery (day 1)
  • Male and Females

Exclusion Criteria

  • Patient refusal
  • Drug abusers and addicts
  • Major significant systemic diseases
  • Language barriers

Outcomes

Primary Outcomes

dynamic and static pain

Time Frame: during the first 24 hours

Pain scores or rest and during movements

postoperative pain scores

Time Frame: first 3 days postoperative

using visual analogue scale (VAS) for pain assessment of 11 points (from "0" no pain to "10" worst pain

time in severe pain

Time Frame: during the first 24 hours

duration of time spent in severe pain after surgery

Secondary Outcomes

  • total analgesic consumption(during the first 24 hours)
  • worst and least pain(during the first 24 hours)
  • time to first request of analgesia(during the first 24 hours)

Study Sites (1)

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