Preoperative Pain Catastrophizing and Intraoperative Analgesia Consumption

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

33 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-04-11

Study Completion Date

2025-07-07

Brief Summary

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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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Detailed Description

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Conditions

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Catastrophizing Pain Pain

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients undergoing laparoscopic cholecystectomy

No interventions assigned to this group

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No