Burns
Conditions
Interventions
Alfentanil group:The optimal dose of alfentanil was determined for continuous pumping
Control group:Continuous pumping of the same volume of normal saline
Sponsors
Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1.Burn patients undergoing wound dressing change; 2.Patients ranged in aged 18 to 65 years; 3.The burn site of the patient is not limited, the burn depth is I-II degree, the burn area is between 1-50%; 4.ASA classification I- III; 5.BMI 18.5 ~ 23.9 kg/m^2; 6.Patient or client signs informed consent.
Exclusion criteria
Exclusion criteria: 1.Patients with a history of mental illness or disorder of consciousness who are unable to cooperate and who use antianxiety drugs or sedatives for a long time (>1 week); 2.Patients with a history of chronic pain (e.g. toothache, stomachache, headache, etc.); 3.Patients with severe organ dysfunction; 4.Patients with inhalation lung injury undergoing tracheotomy and mechanical ventilation; 5.Patients did not survive more than 24 hours after treatment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual analogue scoring;Verbal Rating Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient satisfaction;Total amount of alfentanil application, times and doses of intraoperative alfentanil addition;Whether to use oxygen, airway intervention;Whether other medications are used for intervention; | — |
Countries
China
Contacts
Public ContactZhuang Lei
Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Outcome results
None listed