Pain management after anterior cruciate ligament reconstruction
Conditions
Interventions
Control group:Patients in the control group received conventional pain management and placebo plasters on the basis of basic treatment methods.
Experimental Group:The experimental group was intervened with flurbiprofen gel plaster application on the basis of the control group
Sponsors
West China Hospital of Sichuan University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Adult patients, aged 18-60 years 2. Patients who underwent the procedure for the first time 3. No previous treatment with opioids or psychotropic drugs
Exclusion criteria
Exclusion criteria: 1. Changes in surgical methods caused by various reasons 2. Severe cardiovascular and cerebrovascular diseases (such as uncontrolled hypertension systolic blood pressure > 180mmHg, recent myocardial infarction) 3. Patients with cognitive impairment or a history of psychiatric disorders 4. Patients with a history of allergy to flurbiprofen gel plaster 5. Patients with history of aspirin asthma 6. Forced immobilization due to infection, internal fixation loosening, etc 7. Patients who cannot adhere to complete all treatment and follow-up
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS pain intensity during rehabilitation exercises; | — |
Secondary
| Measure | Time frame |
|---|---|
| The maximum and minimum intensities of resting pain in patients at 24 hours, 48 hours and 72 hours after the operation;The total amount of additional analgesics used;The incidence of side effects of analgesics;The satisfaction of patients with postoperative pain control;A quality of life project disrupted by pain;Whether the blinding of the patient is successful or not; | — |
Countries
China
Contacts
Public ContactLi Pengcheng
West China Hospital of Sichuan University
Outcome results
None listed