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Clinical observation on the function after hip arthroplasty by the combination of meridian tuina manipulation and lymphatic reflux manipulation

Clinical observation on the function after hip arthroplasty by the combination of meridian tuina manipulation and lymphatic reflux manipulation - Clinical observation on the function after hip arthroplasty by the combination of meridian tuina manipulation and lymphatic reflux manipulation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083159
Enrollment
Unknown
Registered
2024-04-17
Start date
2024-04-20
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

Post Hip Replacement

Interventions

Routine group (R) :Routine Rehabilitation, including, physical factor therapy, exercise rehabilitation, each time about 40 minutes, once a day. Exercise rehabilitation: ankle pump training, hip perip
Lymphatic reflux group (L):Lymphatic reflux treatment was performed in the affected side of the inguinal region after conventional rehabilitation, mainly using the pressure delivery maneuver and shove
Push and massage technique group (M):Push and massage technique (M): the threaded surface of the thumb is applied to the skin, the elbow joint is used as the fulcrum, and the forearm is actively swung
Push and massage + Lymphatic reflux group (M+L):Push and massage (M): the thumb threaded surface is applied to the skin, with the elbow joint as the fulcrum, the forearm is actively swung, driving the

Sponsors

Shanghai Fourth People's Hospital, Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Age 60-80 years old, gender is not limited; 2) First time hip arthroplasty; 3) Limited mobility and edema of the lower limbs; 4) Be conscious and have normal cognitive function (MMSE score =26); 5) The patient agrees to be enrolled in the study and signs the clinical informed consent form for participation in the study; 6) Have the ability to complete the relevant tests

Exclusion criteria

Exclusion criteria: 1) Central nervous system diseases, including heart failure and severe cirrhosis with ascites; 2) Preoperative presence of severe deformity, osteomyelitis, joint tuberculosis, joint infection; 3) Combination of other diseases that affect the rehabilitation process after total hip arthroplasty; 4) Inability to cooperate with rehabilitation treatment; 5) Patients who have participated in other related clinical studies within 3 months; 6) Communication problems, such as severe hearing, vision or speech impairment

Design outcomes

Primary

MeasureTime frame
Swelling of the affected limb;

Secondary

MeasureTime frame
Active and passive hip flexion angles;Pain scores;Harris scores;6-minute walk test;

Countries

China

Contacts

Public ContactLi Fei

Shanghai Fourth People's Hospital, Tongji University

1579156025@qq.com+86 186 1612 4115

Outcome results

None listed

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