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Observation of the efficacy of acupuncture in promoting recovery after hip fracture surgery

Observation of the efficacy of acupuncture in promoting recovery after hip fracture surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001644
Enrollment
Unknown
Registered
2025-09-01
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Postoperative hip fracture

Interventions

Sham acupuncture group:Sham acupuncture

Sponsors

Sichuan Suining Third People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1)Post-operative hip fracture patients aged between 50-75 years old male or female; 2) The fracture site is mainly unilateral; 3) The pain level is moderate to severe (4 points = VAS score = 9 points); 4) The first time to receive surgical treatment for hip fracture; 5) The patients can walk normally and take care of their own life before the injury; 6) The patients can actively cooperate with each other to complete the clinical study and sign the informed consent form. (Note: Patients who meet the above 6 items at the same time can be included in this study.)

Exclusion criteria

Exclusion criteria: 1)patients with multiple fractures or pathological fractures; 2) patients with combined cardiovascular cerebrovascular hepatic renal hematopoietic system and other primary diseases and other organic diseases or infections allergies skin diseases etc.; 3) patients with combined severe anxiety depression insomnia and other mental illnesses or intellectual disability who are unable to cooperate with the questionnaires; 4) patients with a history of allergic reactions to opiate analgesic medication; 5) patients who are unable to tolerate acupuncture treatments or who are allergic to acupuncture needles; 6) malignant tumors Patients; 7) Patients who are participating in other programs. (Note: Patients who meet any 1 of the above items will be excluded from this study)

Design outcomes

Primary

MeasureTime frame
Value analogue scale;

Secondary

MeasureTime frame
Self-Rating Anxiety Scale;Lower extremity swelling measurement;Patient satisfaction evaluation;Quality of life score;blinded evaluation;Harris Score;Expected evaluation of treatment effect;Level of inflammatory factors ;Self-Rating Depression Scale;compliance assessment;remedial analgesia rate;

Countries

China

Contacts

Public ContactTianlong Zhang

Sichuan Suining Third People's Hospital

1121709223@qq.com13219206377

Outcome results

None listed

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