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The medial attachment-typed infrapatellar fat pad (IPFP) in total knee arthroplasty (TKA)

The medial attachment-typed infrapatellar fat pad (IPFP) in total knee arthroplasty (TKA)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080357
Enrollment
Unknown
Registered
2024-01-26
Start date
2024-01-29
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

osteoarthropathy

Interventions

"IPFP flap with pedicle medial attachment "group:IPFP was intact during the operation, and the pedicle was medial
"Complete IPFP removal" group:IPFP was completely resected during the operation

Sponsors

The First Affiliated Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Primary Osteoarthritis (OA) (KL grade > =2) 2. Age: 40-80 years old 3. Primary unilateral total knee replacement 4. Patients should voluntarily participate in this study, adopt IPFP flap retention or total IPFP excision method, and sign informed consent

Exclusion criteria

Exclusion criteria: 1. Other surgical procedures: Unicondylar replacement (UKA), high tibial osteotomy (HTO), revision surgery 2. Use the partially reserved IPFP scheme 3. Patients have other diseases or conditions that may affect the results, such as infection, diabetes, rheumatoid arthritis, use of anticoagulants, etc

Design outcomes

Primary

MeasureTime frame
Amount of bleeding;VAS score;knee injury and osteoarthritis outcome score, knee injury and osteoarthritis outcome subscore;

Secondary

MeasureTime frame
Keen Society Score ;range of motion(ROM);C-reactive protein (CRP);ESR;interleukin-6 (IL-6);Length of stay;Incidence of infection;Reoperation rate;Other complications;

Countries

China

Contacts

Public ContactZhang Wenming

The First Affiliated Hospital of Fujian Medical University

zhangwm0591@163.com+86 139 5039 1800

Outcome results

None listed

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