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Clinical observation of a multimodal anesthesia strategy and pain management protocol optimized for daytime total hip arthroplasty

Clinical observation of a multimodal anesthesia strategy and pain management protocol optimized for daytime total hip arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051833
Enrollment
Unknown
Registered
2021-10-06
Start date
2021-10-15
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

analgesia for the total hip arthroplasty patients

Interventions

Group 1:Spinal anesthesia + Fascia iliaca block
Group 2:General anesthesia + Fascia iliaca block

Sponsors

Guizhou Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. Patients with primary total hip arthroplasty (THA); 3. Have the ability to communicate and understand; 4. ASA Class 1-2; 5. BMI = 120g/L; 7. No progressive infection and abnormal coagulation function; 8. Willing to participate in research and be familiar with walking assistance methods and have relatives to take care of them.

Exclusion criteria

Exclusion criteria: 1. Bilateral THA surgery; 2. Have a history of severe heart disease; 3. Insulin-dependent diabetes; 4. History of chronic pain; 5. Failure to comply with the program.

Design outcomes

Primary

MeasureTime frame
Postoperative entry to PACU to discharge time;

Secondary

MeasureTime frame
Postoperative visual analogue scale;Patient recovery quality assessment QoR-15;72-hour postoperative opioid use;30-day postoperative opioid use;Complications within 30 days after surgery;Opioid-related symptom score;Postoperative ambulation time;Hospital stay within 30 days;Readmission 30 days after surgery;

Countries

China

Contacts

Public ContactFang Kaiyun

Guizhou Provincial People's Hospital

fangkaiyun@sina.cn+86 13985533277

Outcome results

None listed

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