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Clinical study on cause analysis of knee pain in patients with hip dysplasia after total hip replacement

Clinical study on cause analysis of knee pain in patients with hip dysplasia after total hip replacement

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091701
Enrollment
Unknown
Registered
2024-11-01
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

Developmental dysplasia of the hip (DDH)

Interventions

Group of patients with developmental hip dysplasia:None

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1.Ages 18-50 2.Patients with hip dysplasia 3.Patients undergoing total hip replacement; 4.The patient has the ability to act autonomously, is willing to follow the study instructions and complete all the required follow-up, and signs the consent form.

Exclusion criteria

Exclusion criteria: 1.The patient has other musculoskeletal abnormalities or neuromuscular diseases; 2.Previous history of external fixation or surgery of the affected limb; 3.Previous history of trauma or infection of the affected limb; 4.Preoperative knee pain (VAS=1 score)

Design outcomes

Primary

MeasureTime frame
VAS pain score of the knee;—

Secondary

MeasureTime frame
Lysholm score of the knee;Leg length;Hip offset;Anatomical parameters of knee joint;Femoral anteversion angle;Ligament relaxation score;—

Countries

China

Contacts

Public ContactXiangpeng Kong

Chinese PLA General Hospital

18810999609@163.com+86 66848810

Outcome results

None listed

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