Postoperative Pain in Adult Patients.

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

620 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-09-21

Study Completion Date

2019-10-31

Brief Summary

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Each surgical intervention associated with even a minor tissue injury is a source of pain which needs to be effectively controlled. Although the Polish national guidelines for post-operative pain management have been published, many patients experience moderate and severe pain in the postoperative period. The aim of this study is (1) to assess pain severity among adult patients after different types of surgeries; (2) to identify demographic and clinical factors associated with postoperative pain.

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Detailed Description

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Conditions

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Pain, Postoperative Surgical Procedures, Operative

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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SURGICAL PROCEDURES ASSOCIATED WITH SLIGHT TISSUE DAMAGE

Observational study

Intervention Type OTHER

Pain assessment, Anxiety assessment, Depression assessment

SURGICAL PROCEDURES ASSOCIATED WITH MODERATE TISSUE DAMAGE

Observational study

Intervention Type OTHER

Pain assessment, Anxiety assessment, Depression assessment

SURGICAL PROCEDURES ASSOCIATED WITH SUBSTANTIAL TISSUE DAMAGE

Observational study

Intervention Type OTHER

Pain assessment, Anxiety assessment, Depression assessment

Interventions

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Observational study

Pain assessment, Anxiety assessment, Depression assessment

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* adult
* elective surgery
* the American Society of Anesthesiologists score 1-3

Exclusion Criteria

* diagnosed mental illness, alcohol abuse disorders, intellectual disability
* traumatic events within the last 6 months (e.g. death, breakdown of a relationship, job loss)
* problems with verbal communication

Minimum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No