← Back to Clinical Trials
Recruiting NCT07449403

NCT07449403 SII Levels Following PENG Block in Hip Arthroplasty

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07449403
Status Recruiting
Phase
Sponsor Poznan University of Medical Sciences
Condition Hip Osteoarthritis
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2026-03-01
Primary Completion 2026-09-01

Eligibility & Interventions

Sex All sexes
Min Age 65 Years
Max Age 100 Years
Study Type INTERVENTIONAL
Interventions
sodium ChlorideRopivacaine 0.2% Injectable Solution

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2026-03-01 with a primary completion date of 2026-09-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This randomized controlled trial evaluates the effect of ultrasound-guided Pericapsular Nerve Group (PENG) block on the Systemic Immune-Inflammation Index (SII) in elderly patients undergoing total hip arthroplasty under spinal anesthesia. SII, calculated as platelet × neutrophil / lymphocyte count, is used as a composite marker of perioperative inflammatory and immune response. The study investigates whether PENG block attenuates the systemic inflammatory reaction to surgical trauma compared to sham block.

Eligibility Criteria

Inclusion Criteria: * Patients with ASA classification I-III * Aged 65-100 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

Frequently Asked Questions

Who can join the NCT07449403 clinical trial?

This trial is open to participants of all sexes, aged 65 Years or older, up to 100 Years, studying Hip Osteoarthritis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07449403 currently recruiting?

Yes, NCT07449403 is actively recruiting participants. Visit ClinicalTrials.gov or contact Poznan University of Medical Sciences to inquire about joining.

Where is the NCT07449403 trial being conducted?

This trial is being conducted at Poznan, Poland.

Who is sponsoring the NCT07449403 clinical trial?

NCT07449403 is sponsored by Poznan University of Medical Sciences. The trial plans to enroll 60 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology