Prospective Observational Study on Postoperative Pain and Side Effect
NCT ID: NCT03808220
Last Updated: 2024-05-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
2197 participants
OBSERVATIONAL
2019-01-20
2021-07-26
Brief Summary
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Detailed Description
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The registry part of the project aims at performing population-based research. Furthermore, its infrastructure allows for the conduct of prospective studies comparing the effectiveness of processes of care.
The benchmark part of the project provides the medical community with a unique, user-friendly system to improve treatment of patients with postoperative pain. A web-based information system, featuring two main functions, was developed:
a feedback and benchmarking system which provides participating sites with continuously updating data and analyses about the quality of care they provide compared to other institutions and allows identification of best clinical practice.
a knowledge library which provides clinicians with easily accessible and regularly updated summaries of evidence-based recommendations tailored to specific post-operative situations.
From 2016 on, sub-projects in Mexico, China and several European countries have started. This programs take place over a period of two years during which collaborators carry out a Quality Improvement project in their hospital using methodology provided by PAIN OUT. This includes collection of baseline data in a first phase, analysis of findings according to a protocol provided by PAIN OUT, review of findings and developement of improvement measures, implementation of the improvements and assessment of outcomes after a second phase of data collection.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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post-surgical patients
post-surgical patients \> 18 years
postoperative pain intensity
estimate the postoperative pain intensity by using a scaling system via questionnaire
preoperative pain frequency
estimate the preoperative pain intensity by using a scaling system via questionnaire
Side effect
investigate the presence of any side effect
pediatric patients post-op day 1
pediatric patients \> 4 years on post-op day 1 (sub-project QUIPSI - PAIN OUTinfant)
postoperative pain intensity
estimate the postoperative pain intensity by using a scaling system via questionnaire
preoperative pain frequency
estimate the preoperative pain intensity by using a scaling system via questionnaire
Side effect
investigate the presence of any side effect
Interventions
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postoperative pain intensity
estimate the postoperative pain intensity by using a scaling system via questionnaire
preoperative pain frequency
estimate the preoperative pain intensity by using a scaling system via questionnaire
Side effect
investigate the presence of any side effect
Eligibility Criteria
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Inclusion Criteria
* patient is post-op day 1
* patient is at least 6 hours on the ward
* patient has given consent
Exclusion Criteria
* patient is cognitively impaired
* patient is asleep
* patient is too ill
* patient does not want to fill in the questionnaire
4 Years
ALL
No
Sponsors
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The University of Hong Kong
OTHER
Responsible Party
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Dr. Chi-Wai Cheung
Professor Cheung Chi Wai
Principal Investigators
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Winfried Meissner
Role: STUDY_DIRECTOR
Jena University Hospital
Chi Wai Cheung, MD
Role: PRINCIPAL_INVESTIGATOR
The University of Hong Kong
Locations
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The University of Hong Kong
Hong Kong, , Hong Kong
Countries
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Other Identifiers
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UW 18-660
Identifier Type: -
Identifier Source: org_study_id
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