Comparing two pain management techniques after knee surgery
The Comparison Of Ultrasound Guıded Adductor Canal Block And Perıcapsular Nerve Group Block For Postoperatıve Analgesıa Management Following Knee Arthroplasty Surgery
This study tests which pain management technique, Adductor Canal Block or Pericapsular Nerve Group Block, works better for people recovering from knee surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Bursa City Hospital Government |
| Locations | 1 site (Bursa) |
| Trial ID | NCT06203483 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of the Adductor Canal Block (ACB) and the Pericapsular Nerve Group Block (PENG) for managing postoperative pain in patients undergoing total knee arthroplasty. As knee arthroplasty surgeries increase, effective pain management is crucial for early mobilization and reducing complications. The study will evaluate how well each technique alleviates pain while preserving motor function, as traditional methods like epidural analgesia and opioids have significant drawbacks. Participants will be monitored for pain relief and mobility post-surgery.
Who should consider this trial
Good fit: Ideal candidates are patients classified as ASA I-II who are scheduled for total knee arthroplasty under spinal anesthesia.
Not a fit: Patients with a history of bleeding disorders, those on anticoagulant therapy, or individuals with allergies to local anesthetics or opioids may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing knee arthroplasty, enhancing recovery and mobility.
How similar studies have performed: Previous studies have shown promising results with similar regional anesthesia techniques, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * American Society of Anesthesiologists (ASA) classification I-II * Scheduled for total knee arthroplasty under spinal anesthesia Exclusion Criteria: * history of bleeding diathesis * receiving anticoagulant treatment, * known local anesthetics and opioid allergy, * infection of the skin at the site of the needle puncture, * pregnancy or lactation, * patients who do not accept the procedur
Where this trial is running
Bursa
- Mürsel Ekinci — Bursa, Turkey (Recruiting)
Study contacts
- Study coordinator: Mursel Ekinci
- Email: drmurselekinci@gmail.com
- Phone: +905067137596
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.