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Optimizing Analgesic Strategy for Elderly Patients with Femoral Neck Fractures Undergoing Total Hip Arthroplasty: A Randomized Controlled Trial on the Optimal Dose of Adrenaline in Cocktail Local Infiltration

Optimizing Analgesic Strategy for Elderly Patients with Femoral Neck Fractures Undergoing Total Hip Arthroplasty: A Randomized Controlled Trial on the Optimal Dose of Adrenaline in Cocktail Local Infiltration

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118676
Enrollment
Unknown
Registered
2026-02-10
Start date
2026-02-10
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

femoral neck fracture

Interventions

0.2 mg epinephrine group:The dose of adrenaline in the cocktail was 0.2 mg.
0.3 mg epinephrine group:The dose of adrenaline in the cocktail was 0.3 mg.
0.4 mg epinephrine group:The dose of adrenaline in the cocktail was 0.4 mg.
0.5mg epinephrine group:The dose of adrenaline in the cocktail was 0.5 mg.

Sponsors

Yuyao Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 65 years old and <= 99 years old ; 2. Garden type III or IV femoral neck fracture was diagnosed by X-ray or CT. 3. Plan to perform primary and unilateral total hip arthroplasty within 72 hours after injury ; 4. American Society of Anesthesiologists grade I-III ; 5. Patients or their legal representatives informed consent, and voluntarily signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Pathological fracture or combined with ipsilateral acetabular, femoral shaft and other serious fractures ; 2. Have a history of ipsilateral hip surgery ; 3. known to be allergic to research drugs ( ropivacaine, compound betamethasone, epinephrine ) or opioids ; 4. Uncontrolled severe systemic diseases ( such as uncontrolled hypertension, coronary heart disease, heart failure, severe arrhythmia, liver and kidney failure ) ; 5. There was a clear history of neurological, mental illness or Alzheimer 's disease before surgery, which could not cooperate with postoperative evaluation ( such as schizophrenia, etc. ) ; 6. Preoperative long-term use of opioids ( > 30 mg / day oral morphine equivalent for > 3 months ) or glucocorticoids ; 7. Active infection or sepsis ; 8. The researchers judged that it was not appropriate to participate in any other situation of this study ( such as the expected survival period < 1 year ).

Design outcomes

Primary

MeasureTime frame
Opioid drug consumption;Postoperative pain level;perioperative bleeding;inflammatory markers;

Secondary

MeasureTime frame
First landing time;First walking distance;

Countries

China

Contacts

Public ContactQiyuan Lu

Yuyao Hospital of Traditional Chinese Medicine

2227059714@qq.com+86 159 9005 5949

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026