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Application of LARS Ligament in Bone Prosthesis Replacement

Not yet recruiting
Conditions
Malignant Tumor
Interventions
Other: LARS ligament and bone prosthesis replacement was performed
Registration Number
NCT05616182
Lead Sponsor
Henan Cancer Hospital
Brief Summary

This is a single-center, prospective, real-world observational study designed to enroll all patients eligible for enrollment. Basic data, treatment methods, postoperative complications and limb function were collected. The differences in postoperative complications, postoperative limb function and so on between patients who underwent LARS ligament implantation and bone prosthesis replacement (ligament group) and patients who underwent bone prosthesis replacement (control group) were compared.

Detailed Description

This is a single-center prospective real-world observational study of 100 eligible patients with bone tumors who are scheduled to undergo LARS ligament implantation and/or bone prosthesis replacement in Henan Cancer Hospital in the next 10 years. Basic data, treatment methods, postoperative complications and limb function were collected. The differences in postoperative complications, postoperative limb function and so on between patients who underwent LARS ligament implantation and bone prosthesis replacement (ligament group) and patients who underwent bone prosthesis replacement (control group) were compared.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria

Men and women of all ages are welcome.

Pathologically confirmed in our hospital as a subtype of malignant tumor.

He received LARS ligament and bone prosthesis replacement at our hospital.

Exclusion Criteria

Not Applicable.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
LARS ligament and bone prosthesis replacement was performedLARS ligament and bone prosthesis replacement was performedTo report the postoperative complications and limb function of patients who underwent LARS ligament and bone prosthesis replacement in Henan Cancer Hospital.
Primary Outcome Measures
NameTimeMethod
Limb functionPatients were enrolled until 24 months after surgery

Limb function was assessed using the Musculoskeletal Oncology Society (MSTS) scoring scale for seven items, namely movement, pain, stability, deformity, strength, functional activity, and emotional receptiveness. The highest possible score is 35, with 5 points allocated to each project.

Postoperative complicationsFrom surgery to 24 months after surgery

Complications of patients undergoing LARS ligament and bone prosthesis replacement.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Department of Bone and Soft Tissue ,Henan Cancer Hospital

🇨🇳

Zhengzhou, Henan, China

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