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OpenTrials
Completed

NCT Number: NCT06838897

Preoperative Pain Catastrophizing and Intraoperative Analgesia Consumption

This observational study aims to evaluate the relationship between the Pain Catastrophizing Scale (PCS) and intraoperative analgesia consumption in patients undergoing laparoscopic cholecystectomy. During the preoperative period, patients will complete the Pain Catastrophizing Scale, the Beck Depression Inventory, and the Beck Anxiety Scale. During the intraoperative period, analgesia nociceptive index (ANI) electrodes will be placed, and remifentanil dosing will be adjusted accordingly. The correlation between preoperative Pain Catastrophizing Scale scores and intraoperative remifentanil consumption will be analyzed.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Samsun Üniversitesi Eğitim Ve Araştırma Hastanesi

Samsun, ilkadım, 55100, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with ASA scores of I-III
  • Patients with Turkish literacy skills.
  • Patients scheduled for elective laparoscopic cholecystectomy.

Exclusion criteria

  • Patients unwillingness to participate in the study.
  • Conversion of surgery from laparoscopic to open surgery.
  • Patients undergoing emergency laparoscopic cholecystectomy.

Treatment and study plan

Primary outcomes

  1. Intraoperative remifentanyl requirement

    Time frame: Intraoperative period

    The main purpose of this study is to evaluate the correlation between preoperative Pain Catastrophizing Scale and intraoperative analgesia consumption.Intraoperative analgesic dose is adjusted according to the analgesia nociceptive index.

Secondary outcomes

  1. Numeric rating scale for postoperative pain intensity

    Time frame: up to 24 hours

    Changes in Numeric Rating Scale (NRS) at rest and on movement will be recorded at intervals. NRS is a unidimensional measure of pain intensity in adults. The NRS is a segmented numeric version of the visual analog scale in which a respondent selectsand its correlation with the preoperative PCS score will be investigated.

Sponsors and collaborators

Lead sponsor

Ahmet Pece

Other

Registry information

Official study title

Association Between Preoperative Pain Catastrophizing Scale and Intraoperative Analgesia Consumption in Elective Laparoscopic Cholecystectomy

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Feb 21, 2025
Registry last updated
Jul 23, 2025

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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