Ultrasound predictors of adductor canal block success after knee replacement
Official title: Ultrasonographic Predictors of Adductor Canal Block Effectiveness in Total Knee Arthroplasty
Run by Konya City Hospital · NCT07730216 · Data updated 2026-11-12
This study tests whether ultrasound factors can predict how well an adductor canal block will relieve pain after total knee arthroplasty in adults.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 623 (estimated) |
| Sponsor | Konya City Hospital Academic / other |
| Locations | 1 site (Konya, Konya) |
| Status | Recruiting |
| Started | August 9, 2026 |
| Main results expected | July 13, 2027 |
| Study ends | July 13, 2027 |
| Registry record updated | August 12, 2026 |
| Trial ID | NCT07730216 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years or older undergoing elective primary unilateral TKA under spinal anesthesia with ASA I–III.
✕Probably not a fit
Patients whose pain control is influenced more by non-ultrasound factors or who have atypical anatomy may not see predictive benefits.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study investigates ultrasound-derived factors, such as tissue depth and injectate spread, to predict the effectiveness of adductor canal blocks for postoperative analgesia after unilateral total knee arthroplasty performed under spinal anesthesia. The aim is to identify imaging characteristics that correlate with reduced need for rescue opioids and better pain control. Eligible participants are adults undergoing elective primary unilateral TKA with ASA I-III. The study analyzes block performance using ultrasound guidance and follows postoperative analgesia outcomes to determine predictive value.
Why it matters
Potential benefit: If successful, ultrasound predictors could help tailor anesthesia plans to improve pain control and reduce opioid use after knee replacement.
How similar studies have gone: Prior research supports ultrasound-guided nerve blocks for accuracy, but predictive ultrasound markers for ACB success specifically are still being explored.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥18 years * Scheduled for elective primary unilateral total knee arthroplasty under spinal anesthesia * American Society of Anesthesiologists (ASA) physical status I-III Exclusion Criteria: * Daily opioid use or chronic pain syndrome * Diabetic or other clinically diagnosed peripheral neuropathy * Coagulopathy * Infection at the injection site * Known allergy or hypersensitivity to local anesthetics * Revision total knee arthroplasty * Conversion from spinal anesthesia to general anesthesia during surgery * General anesthesia as the planned anesthetic technique
Where it's running
-
Konya City Hospital
Konya, Konya, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Ömer Keklicek, Principal Investigator
- Email: drokeklicek@gmail.com
- Phone: +905399291702
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.