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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorDr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital

About this trial

Postoperative pain remains a significant clinical challenge that directly affects patient recovery, functional outcomes, and overall quality of care. Inadequate pain control in the early postoperative period is associated with delayed mobilization, increased risk of complications, prolonged hospital stay, and the development of chronic pain. The post-anesthesia care unit (PACU) represents a critical phase in which pain is actively assessed and managed, and analgesic consumption during this period serves as an objective indicator of analgesic requirements and effectiveness of perioperative pain strategies.

This prospective observational study aims to identify patient-related, surgical, and anesthesia-related factors influencing analgesic consumption in the early postoperative period among adult patients admitted to the PACU following elective surgery. No additional interventions will be performed, and all perioperative management will follow routine clinical practice. Data will be collected prospectively from clinical records, anesthesia charts, and PACU monitoring forms.

The primary outcome is total analgesic consumption during the PACU stay. Secondary outcomes include pain intensity assessed using a standardized pain scale at PACU admission and discharge, requirement for rescue analgesia, incidence of postoperative nausea and vomiting, and length of stay in the PACU.

The findings of this study are expected to contribute to the identification of patients at higher risk for increased analgesic requirements and to support the development of individualized pain management strategies, ultimately improving perioperative care quality and patient outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Patients younger than 18 years

Emergency surgical procedures

Patients transferred directly to the intensive care unit postoperatively

PACU stay shorter than 30 minutes

Trial population

Adult patients undergoing elective surgical procedures and admitted to the post-anesthesia care unit (PACU) in a tertiary oncology hospital. The study population represents a heterogeneous surgical cohort managed under routine perioperative care conditions.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Observational Assessment

    Other intervention

    This is a non-interventional observational study. No experimental intervention is applied. All patients receive routine perioperative care according to institutional clinical practice. The study involves prospective collection and analysis of clinical data related to analgesic consumption and associated factors during the early postoperative period in the post-anesthesia care unit (PACU).

Treatment groups

254 Participants
are divided into 1 treatment group
Group A: PACU Observational Cohort1 intervention

Trial outcomes

Primary outcomes

1

Total Analgesic Consumption in the PACU

Total amount of analgesic medications administered to patients during their stay in the post-anesthesia care unit (PACU). Analgesic consumption will be recorded and standardized (e.g., converted to morphine equivalents if applicable) to allow comparison across patients.

Time frame
During PACU stay (from admission to discharge, within approximately 0-4 hours postoperatively)

Secondary outcomes

1

Pain Intensity at PACU Admission

Pain intensity assessed at admission to the post-anesthesia care unit (PACU) using a standardized pain scale (e.g., Visual Analog Scale or Numeric Rating Scale, 0-10, where 0 indicates no pain and 10 indicates worst imaginable pain).

Time frame
At PACU admission (within the immediate postoperative period)
2

Pain Intensity at PACU Discharge

Pain intensity assessed at discharge from the post-anesthesia care unit (PACU) using a standardized pain scale (e.g., Visual Analog Scale or Numeric Rating Scale, 0-10).

Time frame
At PACU discharge (within approximately 0-4 hours postoperatively)
3

Requirement for Rescue Analgesia in the PACU

Need for additional rescue analgesic treatment during PACU stay, recorded as whether rescue analgesia was required.

Time frame
During PACU stay (from admission to discharge, within approximately 0-4 hours postoperatively)
4

Incidence of Postoperative Nausea and Vomiting in the PACU

Occurrence of postoperative nausea and/or vomiting during PACU stay, recorded based on routine clinical assessment.

Time frame
During PACU stay (from admission to discharge, within approximately 0-4 hours postoperatively)

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.