Clinical trial Recruiting at 1 site Observational Ages 18 and up

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.

More Arthroplasty, Replacement, Knee trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment623 (estimated)
SponsorKonya City Hospital
Academic / other
Locations1 site (Konya, Konya)
StatusRecruiting
StartedAugust 9, 2026
Main results expectedJuly 13, 2027
Study endsJuly 13, 2027
Registry record updatedAugust 12, 2026
Trial IDNCT07730216 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.