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In the preemptive analgesia mode: a randomized controlled study of pregabalin combined with celecoxib in total knee arthroplasty

In the preemptive analgesia mode: a randomized controlled study of pregabalin combined with celecoxib in total knee arthroplasty

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100041595
Enrollment
Unknown
Registered
2021-01-01
Start date
2021-01-05
Completion date
Unknown
Last updated
2021-06-22

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

Conditions

Total knee replacement

Interventions

placebo group:placebo 350mg
celecoxib:celecoxib 200mg
pregabalin group:pregabalin 150mg
Joint Group:Celecoxib 200mg+ Pregabalin 150mg

Sponsors

The Third Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
46 Years to 72 Years

Inclusion criteria

Inclusion criteria: 1. Patients over 50 years old and under 80 years old will undergo elective, primary, unilateral total knee arthroplasty; 2. Patients with ASA physical condition below grade 3 of American Society of anesthesiologists; 3. Patients who are willing to participate in this study and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with history of liver and kidney insufficiency, severe cardiopulmonary disease, severe digestive tract disease and psychosis; 2. Patients allergic to celecoxib and pregabalin; 3. Patients who had taken celecoxib and pregabalin within one week before operation.

Design outcomes

Primary

MeasureTime frame
VAS??;Cumulative dosage of opioid receptors;

Countries

China

Contacts

Public ContactXiang Bingyan

The Third Affiliated Hospital of Zunyi Medical University (Zunyi First People's Hospital)

xby1978@126.com+86 18685239990

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026