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Clinical study for the effect of preoperative analgesia on total knee replacement on postoperative rehabilitation

Clinical study for the effect of preoperative analgesia on total knee replacement on postoperative rehabilitation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027892
Enrollment
Unknown
Registered
2019-12-02
Start date
2018-10-01
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

Knee osteoarthritis

Interventions

Buprenorphine group:Buprenorphine transdermal patch 2.5mg applied to deltoid muscle 12h before surgery
Celecoxib group:Celecoxib 200mg orally 12h before surgery
Blank control group:No advanced analgesia

Sponsors

Lanzhou University Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: The patients undergoing first total knee arthroplasty performed by the same group of surgeons still had moderate to severe pain (NRS score of sports pain> 3) in the outpatient follow-up after discharge (1 month after surgery) and the patients gave informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of severe cardiopulmonary and cerebrovascular diseases, patients with abnormal liver and kidney function, patients with active peptic ulcer or gastrointestinal bleeding; 2. Patients allergic to opioids and sulfa drugs; 2. Patients with hip joint disease, lumbar spine disease, neurogenic pain and other comorbidities; 3. Have a long history of COX-2 inhibitors and opioids; 4. Patients with deep infection or deep vein thrombosis in the early postoperative period; 5. Patients who cannot cooperate with follow-up and rehabilitation guidance.

Design outcomes

Primary

MeasureTime frame
pain(Mean resting pain and movement pain);Knee flexion and extension;drug's adverse reactions;

Countries

China

Contacts

Public ContactYin Xiaoli

Lanzhou University Second Hospital

2292146781@qq.com+86 13919092460

Outcome results

None listed

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