Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Does implant type affect knee alignment when using KUNWU robotic surgery

Official title: Comparison of Postoperative Knee Alignment to Planned Alignment Using Two Implant Types and a Novel Robotic Platform in Total Knee Replacement - A Randomized Controlled Trial

Run by The University of Hong Kong · NCT07777757 · Data updated 2026-11-12

This trial tests whether two knee implants (Attune vs Persona) used with the KUNWU robotic system result in more accurate knee alignment after total knee replacement.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorThe University of Hong Kong
Academic / other
Locations1 site (Hong Kong, Sandy Bay)
StatusRecruiting
StartedMarch 18, 2026
Main results expectedSeptember 30, 2028
Study endsDecember 31, 2028
Registry record updatedAugust 21, 2026
Trial IDNCT07777757 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with symptomatic knee osteoarthritis requiring total knee replacement who can tolerate either Attune or Persona implants and meet study criteria.

Probably not a fit

Patients for whom alignment with either implant does not meet the planned targets or who experience implant-related complications may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a single-center, randomized, double-blind study evaluating two commercial knee implants—Attune and Persona—used with a novel CT-based KUNWU robotic system for total knee replacement in adults with knee osteoarthritis. Participants are randomly assigned to receive one of the two implants, while patients and outcome assessors remain unaware of the implant choice. All surgeries are performed by a single team using the KUNWU system to follow preoperative CT plans and achieve target alignment. The primary outcome is the accuracy of postoperative knee alignment relative to the preoperative plan; secondary considerations include safety and surgical workflow. Enrollment is limited to eligible adults at The Duchess of Kent Children’s Hospital in Hong Kong, with standard inclusion/exclusion criteria.

Why it matters

Potential benefit: If successful, patients may benefit from improved implant alignment, which could contribute to better joint function and potentially longer implant life.

How similar studies have gone: Other robotic-assisted knee replacement studies have shown benefits in accuracy with robotic guidance, though results can vary by system and implant type.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults aged 18 years and older.
* Diagnosis of symptomatic knee osteoarthritis requiring total knee replacement.
* Ability to give informed consent.
* Feasibility of using the two types of implants

Exclusion Criteria:

\- Severe radiographic knee OA (Kellgren-Lawrence grade 4) or severe knee pain (VAS\>80mm/100 mm) that could not tolerate further conservative management

Where it's running

  • The Duchess of Kent Children's Hospital at Sandy Bay
    Hong Kong, Sandy Bay, Hong Kong
    Recruiting

Study contacts

  • Study coordinator: Chun Man Lawrence Prof. Lau, MBChB, MRCSEd, FRCSEd(Orth), F
  • Email: laucml@hku.hk
  • Phone: 92646862

Similar studies

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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.