Postoperative sore throat
Conditions
Interventions
Experimental group:Conventional Treatment+ Traditional Chinese Medicine Acupoint Patch Therapy
Control group:Conventional Treatment + Placebo Patches
Sponsors
The First Hospital of Lanzhou University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: ? surgical patients undergoing general anaesthesia via orotracheal intubation; ? patients aged 18-60 years old; ? patients with Body Mass Index (BMI) 60min; ? postoperative users of intravenous self-control analgesic pumps; and ? voluntary participation and signing of an informed consent form.
Exclusion criteria
Exclusion criteria: ?People with a history of respiratory tract infection or sore throat in the two weeks before surgery; ?People who are allergic to Salvia divinorum, Cynanchum officinale, Silybum marianum, Glycyrrhiza glabra, or adhesive tape; ?People whose acupoints are located in a position where it is impossible for them to apply the tape (e.g., trauma, ulcers, and infections); ?People who are classified as grade III-IV in the Mallampati Classification; ?People who suffer from severe diabetes mellitus or pregnant women; and ?people who are conscious of the disorder and have poor communication skills.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of postoperative sore throat at 24h; | — |
Secondary
| Measure | Time frame |
|---|---|
| Use of postoperative analgesic drugs;Severity of sore throat;Cough incidence;Incidence of sputum;Patient satisfaction with the effectiveness of combating postoperative sore throat;Incidence of postoperative sore throat at 48h;Incidence of hoarseness; | — |
Countries
China
Contacts
Public ContactFan Luo
The First Hospital of Lanzhou University
Outcome results
None listed