Application of LARS Ligament in Bone Prosthesis Replacement

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorHenan Cancer Hospital

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Patients undergoing LARS ligament and bone prosthesis replacement

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • LARS ligament and bone prosthesis replacement was performed

    Other intervention

    To report the postoperative complications and limb function of patients who underwent LARS ligament and bone prosthesis replacement in Henan Cancer Hospital.

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: LARS ligament and bone prosthesis replacement was performed1 intervention

Trial outcomes

Primary outcomes

1

Postoperative complications

Complications of patients undergoing LARS ligament and bone prosthesis replacement.

Time frame
From surgery to 24 months after surgery
2

Limb function

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.

Time frame
Patients were enrolled until 24 months after surgery

Secondary outcomes

Other outcomes

Sponsors and contacts

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