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Metabolic and inflammatory responses and subsequent recovery in traditional total hip arthroplasty and mechanical arm assisted total hip arthroplasty

Metabolic and inflammatory responses and subsequent recovery in traditional total hip arthroplasty and mechanical arm assisted total hip arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061346
Enrollment
Unknown
Registered
2022-06-21
Start date
2022-06-08
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diseases with indications for total hip arthroplasty

Interventions

control group:traditional total hip arthroplasty

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age 18 ~ 80 years old, regardless of gender; 2.Patients who meet the requirements of total hip arthroplasty and need the primary total hip arthroplasty according to the evaluation of the researchers; 3.The subjects fully understand the benefits and risks of this trial and are willing to participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients with neuromuscular dysfunction (e.g. paralysis, myolysis or abductor weakness) that can lead to postoperative hip instability or abnormal gait; 2.Active infection lesions in the hip joint or other parts of the body; 3.Patients with severe hip deformity and hip dysplasia with Crowe grade 3 or 4; 4. Ankylosing spondylitis patients with bony ankylosis or severe stiffness; 5. Patients with bilateral hip arthroplasty at the same time, or patients with contralateral hip arthroplasty within 3 months, or patients with contralateral hip arthroplasty expected to be performed within 1 year after operation; 6. The patient is known to have a history of allergy to one or more implanted materials; 7. Patients with severe internal and surgical diseases or weak physiques and unable to tolerate surgery; 8. Patients with poor expected compliance; 9. Pregnant or lactating women, or patients with family planning during clinical research; 10. The patient participating in other drug clinical trials within 3 months before enrollment, or other device clinical trials within 1 month before enrollment; 11.Patients with insulin resistance caused by diabetes or drugs; 12. Other circumstances that the researchers consider inappropriate for participation in the study.

Design outcomes

Primary

MeasureTime frame
Insulin resistance index(HOMA-IR(HOMA-IR 1 day after surgery );

Secondary

MeasureTime frame
Fasting blood glucose (one day before and after operation);Fasting insulin (one day before and after operation);Islet of Langerhans ß Cellular function;Insulin sensitivity index;CRP (within 7 days before operation, 6 hours after operation, 1 day after operation, 3 days after operation, 21 days after operation);ESR (within 7 days before operation, 6 hours after operation, 1 day after operation, 3 days after operation, 21 days after operation);IL-6 (within 7 days before operation, 6h after operation, 1 day after operation, 3 days after operation and 21 days after operation);Cortisol (within 7 days before operation, 6 hours after operation, 1 day after operation, 3 days after operation and 21 days after operation);Serum amyloid A (within 7 days before operation, 6 hours after operation, 1 day after operation, 3 days after operation and 21 days after operation);Active hip flexion angle (within 7 days before operation, 3 days after operation and 21 days after operation);Active hip abduction angle (within 7 days before operation, 3 days after operation and 21 days after operation);Straight leg raising time (within 7 days before operation, 3 days after operation and 21 days after operation);VAS score (within 7 days before operation, 1 day after operation, 2 days after operation, 3 days after operation, 21 days after operation);Intraoperative bleeding;Postoperative drainage;Total postoperative bleeding;

Countries

China

Contacts

Public ContactZongke Zhou
2584045239@qq.com+86 18980601028

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026