Acute Postoperative Pain Prevalence and Intensity in the First 72 Hours

NCT ID: NCT06065683

Last Updated: 2023-10-10

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 350 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2022-09-01
• Study Completion Date: 2023-07-30

Brief Summary

Postoperative pain is poorly studied in developing countries. Severe pain after surgery remains a major problem, occurring in 50% to 70% of the patients. Differences exist across countries. Despite numerous published studies, the degree of pain following many types of surgery in everyday clinical practice is unknown. To improve postoperative pain treatment and develop procedure-specific, optimized pain-treatment protocols, the prevalence and severity of postoperative pain must first be identified.

This study aimed to determine the incidence and intensity of acute postoperative pain, to identify populations associated with a higher risk in order to guide resource allocation, and to investigate whether inexpensive analgesic modalities are currently utilized maximally.

Detailed Description

Postoperative pain management remains one of the major challenges in the care of surgical patients in many parts of the world. Despite improved care, studies show that postoperative pain continues to be inadequately treated and that patients still suffer moderate to severe pain after surgery. Despite an improved understanding of pain mechanisms, several risk factors, and advances in pain management strategies, postoperative pain continues to be a widespread and unresolved problem.

In Ethiopia, pain management is done in the traditional way, and pain control regimens vary from center to center and again from person to person in the same center due to a lack of pain management protocol. Overall pain management criteria used are not clear and sometimes decisions may be influenced by what is available in stock. Therefore, this research on the assessment of postoperative pain management provides information for clinicians to formulate protocols for the management of postoperative pain and for hospital managers in order to guide resource allocation to use limited resources efficiently and plan for optimum postoperative pain management.

In the study, the investigators used a numerical pain rating scale for pain immediately after surgery for the first 72 hours after surgery. The prevalence of mild, moderate, or severe pain and median pain scores were calculated. An evaluation will be performed at eight time points: at T2, T4, T8, T12, T24, T48, and T72. They consider 350 patients from all surgical wards. All surgical procedures were assigned to 5 well-defined groups. When a group contained less than 20 patients the data was excluded from the analysis.

Conditions

Post Operative Pain

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

T2 hour

surgery

Intervention Type: PROCEDURE

Surgical procedures performed in the study period

T12 hour

surgery

Intervention Type: PROCEDURE

Surgical procedures performed in the study period

T24 hour

surgery

Intervention Type: PROCEDURE

Surgical procedures performed in the study period

T48 hour

surgery

Intervention Type: PROCEDURE

Surgical procedures performed in the study period

T72 hour

surgery

Intervention Type: PROCEDURE

Surgical procedures performed in the study period

Interventions

surgery

Surgical procedures performed in the study period

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Age ≥18 years old
• Able to provide informed consent
• Able to verbalize or indicate pain by using a traditional verbal scale such as the numeric rating scale at the 2nd hr. of Post anesthesia care unit arrival.

Exclusion Criteria

• Patients unable to self-report acute pain
• Patients with a history of chronic pain, moderate to high acute pain previous to surgery.
• Patients with a previous diagnosis of chronic cognitive impairment (Dementia, Alzheimer …)
• Patients with a previous diagnosis of Neurologic impairment (paraplegia, q quadriplegia…)
• The patients excluded from the study will be patients with mental and psychological problems.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Wollo University

OTHER

Sponsor Role: lead

Responsible Party

Sara Timerga

Lecturer

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Sara Timerga

Role: PRINCIPAL_INVESTIGATOR

Wollo University

Locations

Wollo Univeersity

Dessie, , Ethiopia

Countries

Ethiopia

Other Identifiers

Acute pain

Identifier Type: -

Identifier Source: org_study_id