A prospective, observational study to assess the functional recovery, duration of hospital stay, and complications in patients undergoing Robot assisted Uni-compartmental Knee Replacement surgery

Recruitment & Eligibility

Status: Open to Recruitment

Sex: All

Target Recruitment: 50

Inclusion Criteria

1.Patients with unicondylar arthritis eligible for Uni-compartmental knee arthroplasty.
2.Male and female aged 45 years and above 3.Subject is willing to take part in the study by signing Ethics Committee (EC) approved informed consent form (ICF) 4.Subjects agrees to comply with postoperative scheduled clinical and radiographic evaluation.

Exclusion Criteria

1.Patient with an active infection within the affected knee joint 2.Patient with neuromuscular or neurosensory deficiency that may affect the ability to evaluate the study end points.
3.Patients who are known drug or alcohol abusers or with psychological disorders that could affect follow up care or treatment outcomes.
4.Patients with history of deep vein thrombosis or other thrombotic disorders.
5.Patients with Inflammatory arthropathy, Previous High tibial osteotomy (HTO) with overcorrection, Cruciate ligament lesion, Medial or lateral subluxation (usually associated with a torn ACL), Tibial or femoral shaft deformity, Flexion contracture greater than 15Â°, Varus deformity greater than 15Â° (medial UKA), Valgus deformity greater than 20Â° (lateral UKA), Flexion less than 110Â°, patellofemoral joint arthritis, obesity, chondrocalcinosis, and crystalline arthropathy 6.Clinical signs of a coexisting severe acute systemic illness (Pneumonia, sepsis, UTI, other co-morbidities) 7.Diagnosis of immune deficiency (AIDS, other congenital immunodeficiency syndrome, drug therapy with steroids, anticancer drugs etc.) 8.Participation in another clinical study within 30 days before the beginning or anytime during the duration of the current clinical study.
9.Patient is unlikely to adhere to study procedures, keep appointments, or is planning to relocate during the study.
10.Any other reason that in the opinion of the investigator may interfere with the evaluation required by the study.
11.Patient identified as employee of the Investigator or study center as well as family members (i.e. immediate, husband, wife and their children, adopted or natural) of the employees or the Investigator.

Study & Design

Study Type: Observational

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To observe the functional recovery, duration of hospital stay and complications of Robotic assisted technology in patients undergoing UKA.	Baseline, 5 days post surgery, 6 weeks, 3 and 6 months, 1 year, 2 year, 3 year and 5 year

Secondary Outcome Measures

Name	Time	Method
Changes in pain levels as reported by patients between pre-operation and post-operation during the course of the study (before discharge and post-surgery	Total time taken for surgery

Trial Locations

Locations (1): Anup Institute of Orthopedics and Rehabilitation
🇮🇳
Patna, BIHAR, India
Anup Institute of Orthopedics and Rehabilitation
🇮🇳Patna, BIHAR, India
Dr Ashish Singh
Principal investigator
8294240349
drashishsingh@hotmail.com