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A non-opioid multimodal analgesia protocol to promote rapid recovery of patients undergoing total hip or total knee arthroplasty: a randomized controlled clinic study

A non-opioid multimodal analgesia protocol to promote rapid recovery of patients undergoing total hip or total knee arthroplasty: a randomized controlled clinic study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050340
Enrollment
Unknown
Registered
2021-08-26
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

hip and knee joints

Interventions

Multimodal hip analgesia group:Non-opioid multimodal analgesia protocol
Multimodal knee analgesia group:Non-opioid multimodal analgesia protocol

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 old; 2.ASA I~III; 3.Elective hip and knee surgery.

Exclusion criteria

Exclusion criteria: 1.Emergency surgery; 2.Respiratory failure and heart function NYHA>=3; 3.liver failure and renal failure require dialysis.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale of postoperative pain;Postoperative opioid use;—

Secondary

MeasureTime frame
Length of hospital stay;30-day readmission rate;Complications as assessed by the incidence of a composite of major complications and a second composite of minor complications.;The 15-item quality of recovery scale was evaluated 30 days after surgery;Postoperative ambulation time;Postoperative feeding time;Postoperative nausea and vomiting;—

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