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NCT Number: NCT07547618

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

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

Ankara, Yenimahalle, 06200, Turkey (Türkiye)

Location status: Recruiting

Location contact

Mustafa Kemal SAHIN, Dr

CONTACT

[email protected]

+905075800976

About this study

Postoperative pain is a major clinical concern that significantly affects recovery, patient satisfaction, and overall perioperative outcomes. 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 postoperative pain. Therefore, early identification of factors influencing analgesic requirements is essential for optimizing individualized pain management strategies.

The post-anesthesia care unit (PACU) represents a critical period during which patients are closely monitored following surgery, and pain management is actively adjusted. Analgesic consumption during this phase provides an objective and clinically relevant measure of pain management adequacy. However, analgesic requirements may vary widely depending on patient-related factors (such as age, sex, and body mass index), surgical characteristics (type and duration of surgery), and anesthesia-related variables (anesthetic technique, intraoperative analgesic administration, and use of regional anesthesia).

This study is designed as a single-center, prospective observational study conducted in the post-anesthesia care unit of a tertiary oncology hospital. Adult patients undergoing elective surgical procedures will be included. No additional interventions will be performed, and all perioperative care will be administered according to routine clinical practice. Data will be collected prospectively from anesthesia records, PACU monitoring forms, and hospital electronic systems.

The primary outcome is total analgesic consumption during the PACU stay. Secondary outcomes include pain intensity 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 in the early postoperative period. These results may support the development of individualized and more effective pain management strategies and improve overall perioperative care quality.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

Observational Assessment

Other

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).

Primary outcomes

  1. Total Analgesic Consumption in the PACU

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

    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.

Secondary outcomes

  1. Pain Intensity at PACU Admission

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

    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).

  2. Pain Intensity at PACU Discharge

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

    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).

  3. Requirement for Rescue Analgesia in the PACU

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

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

  4. Incidence of Postoperative Nausea and Vomiting in the PACU

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

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

  5. Length of Stay in the PACU

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

    Duration of time spent in the post-anesthesia care unit, measured in minutes from PACU admission to discharge.

Study contacts

Contact information is provided by the study sponsor or research team.

Mustafa Kemal Şahin

CONTACT

[email protected]

+905075800976

Sponsors and collaborators

Lead sponsor

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 23, 2026
Registry last updated
Apr 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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