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A prospective randomized controlled study of early rehabilitation after knee arthroplasty with different administration methods of glucocorticoids

A prospective randomized controlled study of early rehabilitation after knee arthroplasty with different administration methods of glucocorticoids

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062701
Enrollment
Unknown
Registered
2022-08-15
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

Knee arthroplasty

Interventions

control group:no dexamethasone use
Experimental group 1:Intravenous administration of dexamethasone 10mg mixed with normal saline to 10ml + local infiltration of knee joint injection of 100mg ropivacaine mixed with normal saline to 50m
experimental group 2:The patient was given 10ml of normal saline intravenously + 100mg of ropivacaine and 10mg of dexamethasone mixed with normal saline to 50ml for local infiltration of knee joint
experimental group 3:Intravenous administration of dexamethasone 5mg mixed with normal saline to 10ml + local infiltration of knee joint injection of 100mg ropivacaine, 5mg dexamethasone mixed with no

Sponsors

Beijing Jishuitan Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Select patients over 50 years old and under 80 years old who received unilateral knee arthroplasty in our hospital from August 2022 to February 2023; 2. Patients diagnosed with osteoarthritis; 3. ASA I to II; 4. The patient has the ability of independent behavior, understands and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients who are allergic to local anesthetics; 2.Patients with rheumatoid arthritis, ankylosing spondylitis and other inflammatory joint diseases; 3. Patients who have used glucocorticoids in the past 1 year; 4. Patients who used opioids in the past; 5. Patients with liver and kidney insufficiency (ALT or AST> 40U/L, serum creatinine > 133umol/L); 6. Contraindications to local infiltration anesthesia; 7. Patients with chronic pain other than knee joint and ineffective conservative treatment; 8. For patients with severe diabetes, the preoperative glycosylated hemoglobin was more than 7%; 9. Other situations that researchers think are not suitable for participation.

Design outcomes

Primary

MeasureTime frame
VAS(Visual Analog Scale) score;

Secondary

MeasureTime frame
Opioid equivalent;Postoperative nausea and vomiting times;Knee range of motion;

Countries

China

Contacts

Public ContactHongyi Shao
jsszshy@163.com+86 13811251845

Outcome results

None listed

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