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Clinical Trials/NCT05558553
NCT05558553CompletedNot Applicable

Are Neutrophil-Lymphocyte Ratio, Platelet-Lymphocyte Ratio, and Systemic Immune Inflammation Score Values Indicators for Postoperative Pain?

Samsun University2 sites in 1 country2 target enrollmentStarted: September 18, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
2
Locations
2
Primary Endpoint
postoperative analgesic consumption

Study Overview

Brief Summary

Postoperative pain status of patients who underwent elective laparoscopic cholecystectomy.

Detailed Description

Subject Researched:

Postoperative pain is a result of the inflammatory response to surgical trauma. Local inflammatory mediator response triggered by surgical incision, dissection, retraction, etc. causes an increase in nociceptor sensitivity and hyperalgesia, resulting in the perception of postoperative pain. With the acute phase response caused by surgical trauma, tissue damage is brought under control, infection is limited and the healing process begins. During the inflammatory response, the level of leukocytes in the blood also changes. Neutrophil/Lymphocyte ratio (NLR), Platelet/Lymphocyte ratio (PLR) and Systemic immune inflammation score (SII) are inexpensive and easily accessible biomarkers calculated from routine hemogram parameters and shown to be helpful in disease investigations and evaluation of treatment response. In this study, the relationship between biomarkers and postoperative pain status due to surgery will be investigated

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients aged 18-75 years who underwent elective laparoscopic cholecystectomy.
  • •Patients with ASA status1-2-3

Exclusion Criteria

  • •Emergency operated patients
  • •Patients switched to open surgery
  • •Patients allergic to tramadol
  • •Those allergic to paracetamol
  • •Those allergic to tenoxicam
  • •Patients who cannot use the patient-controlled analgesia device
  • •Those with hematological disorders
  • •Those receiving immunosuppressive therapy
  • •Those with inflammatory disease
  • •Those with gastrointestinal tumors
  • •Those with rheumatic disease
  • •Those with uncontrolled diabetes
  • •Those with chronic organ failure
  • •Those who use corticosteroids
  • •Opioid users
  • •Those who have recently had an attack of cholecystitis, pancreatitis

Outcomes

Primary Outcomes

postoperative analgesic consumption

Time Frame: 24 hours

Secondary Outcomes

  • postoperative pain score(24 hours)

Investigators

Sponsor
Samsun University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Senay Canikli

medical specialist (Anesthesiology and Reanimation)

Samsun University

Study Sites (2)

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