Actively Recruiting

Age: 18Years +
All Genders
ID07547618

Factors Influencing Analgesic Consumption in the Early Postoperative Period: A Prospective Observational Study in the Post-Anesthesia Care Unit

Led by Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital · Updated on 2026-04-30

254

Participants Needed

1

Research Sites

2 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Postoperative pain is a significant challenge that affects recovery, patient outcomes, and quality of care. Inadequate pain control soon after surgery can delay movement, increase complications, extend hospital stays, and may lead to chronic pain. This prospective observational study aims to identify patient, surgical, and anesthesia factors that influence pain medication use during the early postoperative period in adult patients admitted to the post-anesthesia care unit (PACU) after elective surgery. The study includes a single group of adult patients undergoing elective surgery and monitored in the PACU. No experimental treatments are given; all care follows routine clinical practice. Researchers will collect data on pain medication use, pain intensity, and related factors from clinical records and monitoring forms during the PACU stay, which typically lasts up to four hours after surgery. Participants will be observed during their PACU stay where pain levels at admission and discharge will be recorded using a standardized scale. Researchers will track total pain medication use, need for extra pain relief, episodes of nausea or vomiting, and length of PACU stay. The study focuses on understanding which factors affect pain medication needs to help improve individualized pain management and overall perioperative care. The total observation period in the PACU is approximately 0 to 4 hours postoperatively.

CONDITIONS

Brief Title

Analgesic Consumption in the Early Postoperative Period: A Prospective Observational PACU Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years and older
  • Undergoing elective surgical procedures
  • Admitted to the post-anesthesia care unit (PACU) after surgery
  • Receiving general and/or regional anesthesia
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Patients younger than 18 years
  • Emergency surgical procedures
  • Patients transferred directly to the intensive care unit postoperatively
  • PACU stay shorter than 30 minutes
  • Patients unable to communicate or assess pain
  • Incomplete clinical records
  • Refusal to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 4 hours postoperatively

Participants are observed in the post-anesthesia care unit (PACU) to monitor analgesic consumption and pain during the early postoperative period.

Continuous monitoring during PACU stay

Trial Site Locations

Total: 1 location

1

Dr. Abdurrahman Yurtaslan Ankara Oncology Education and Research Hospital Clinic of Anesthesiology and Rea

Ankara, Yenimahalle, Turkey (Türkiye), 06200

Actively Recruiting

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Research Team

M

Mustafa Kemal Şahin

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Postoperative pain experience: results from a national survey suggest postoperative pain continues to be undermanaged.

Jeffrey L Apfelbaum, Connie Chen, Shilpa S Mehta...

https://pubmed.ncbi.nlm.nih.gov/12873949