FindTrial
Sign In

Comparison of the analgesic effect of ropivacaine in combination with morphine and betamethasone or adductor canal block in total knee arthroplasty without tourniquet: a prospective randomized controlled trial

Comparison of the analgesic effect of ropivacaine in combination with morphine and betamethasone or adductor canal block in total knee arthroplasty without tourniquet: a prospective randomized controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021385
Enrollment
Unknown
Registered
2019-02-18
Start date
2019-02-19
Completion date
Unknown
Last updated
2019-02-25

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

Conditions

Total Knee Arthroplasty

Interventions

A:Ropivacaine in combination with Morphine and Betamethasone
B:Ropivacaine in combination with Morphine and Betamethasone or Adductor Canal Block

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Aged 18 to 85 years, Undertake total knee arthroplasty; Informed consent is available.

Exclusion criteria

Exclusion criteria: Drug allergy.

Design outcomes

Primary

MeasureTime frame
Function outcomes;Pain;Complication;Postoperative analgesic use;—

Countries

China

Contacts

Public ContactZongke Zhou

West China Hospital, Sichuan University

luozhenyu@outlook.it+86 13207100126

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026