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Completed

NCT Number: NCT07023107

NLR and PLR Levels Following PENG Block in Hip Arthroplasty

Effect of PENG block on NLR and PLR following hip arthroplasty

Completed

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Key information

Age range

60 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Poznan University of Medical Sciences

Poznan, Poland

About this study

The NLR is a sensitive indicator of inflammation confirmed in numerous studies and has a predictive and prognostic value. NLR is a cheap, simple, fast-acting, readily available stress and inflammation parameter with high sensitivity and low specificity. Dynamic changes in the NLR precede the clinical state by several hours and may alert clinicians to the ongoing pathological process early. NLR is a new promising marker of cellular immune activation, an important indicator of stress and systemic inflammation. It opens a new dimension for clinical medicine, enabling a better understanding of the biology of inflammation, the linkage and antagonism between innate and adaptive immunity, and their clinical consequences for health and disease.

NLR is affected not only by surgical trauma but also by the method of anesthesia. In recent years, the influence of regional anesthesiology on reducing the inflammatory response after surgical procedures has been emphasized. However, there have been very few studies evaluating the effect of various methods of anesthesia on the NLR.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with ASA classification I-III
  • Aged 60-100 years
  • Who will be scheduled for hip arthroplasty under spinal anesthesia

Exclusion criteria

  • Patients who have a history of bleeding diathesis
  • Take anticoagulant therapy
  • History of chronic pain before surgery
  • Multiple trauma
  • patients unable to assess their pain (dementia)
  • patients operated under general anesthesia
  • patients having an infection in the region of the procedure
  • the patient who does not accept the procedure

Treatment and study plan

0.9% sodium chloride injection

Drug

After spinal anesthesia, the ultrasound-guided PENG block will be performed with 20ml of 0.9% sodium chloride

Ropivacaine 0.2% Injectable Solution

Drug

After spinal anesthesia, the ultrasound-guided PENG block will be performed with 20 ml of 0.2% ropivacaine

Primary outcomes

  1. Neutrophil-to-lymphocyte ratio

    Time frame: 12 hours after surgery

    Neutrophil to lymphocyte ratio (NLR) is used as a marker of subclinical inflammation. It is calculated by dividing the number of neutrophils by number of lymphocytes, usually from peripheral blood sample, but sometimes also from cells that infiltrate tissue, such as tumor.

Secondary outcomes

  1. PLR

    Time frame: 12 hours after surgery

    Platelet-to-lymphocyte ratio

  2. PLR

    Time frame: 24 hours after surgery

    Platelet-to-lymphocyte ratio

  3. PLR

    Time frame: 48 hours after surgery

    Platelet-to-lymphocyte ratio

  4. NLR

    Time frame: 24 hours after surgery

    Neutrophil-to-lymphocyte ratio

  5. NLR

    Time frame: 48 hours after surgery

    Neutrophil-to-lymphocyte ratio

  6. first need of opiate

    Time frame: 48 hours after procedure

    Time after surgery when the patient needs opiate for the first time

  7. Opioid Consumption

    Time frame: 48 hours after surgery

    Total opiate consumption after surgery

  8. Pain score

    Time frame: 4 hours after surgery

    NRS (Numerical Rating Scale) - ranging from 0 to 10, where 0 represents "no pain" and 10 represents the "worst pain imaginable"

  9. Pain score

    Time frame: 8 hours after surgery

    NRS (Numerical Rating Scale) - ranging from 0 to 10, where 0 represents "no pain" and 10 represents the "worst pain imaginable"

  10. Pain score

    Time frame: 12 hours after surgery

    NRS (Numerical Rating Scale) - ranging from 0 to 10, where 0 represents "no pain" and 10 represents the "worst pain imaginable"

  11. Pain score

    Time frame: 24 hours after surgery

    NRS (Numerical Rating Scale) - ranging from 0 to 10, where 0 represents "no pain" and 10 represents the "worst pain imaginable"

Sponsors and collaborators

Lead sponsor

Poznan University of Medical Sciences

Other

Registry information

Official study title

Pericapsular Nerve Group Block Mitigates Surgical Stress and Enhances Analgesia in Total Hip Arthroplasty: A Randomized Controlled Trial

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jun 15, 2025
Registry last updated
Dec 29, 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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