Pterygium
Conditions
Interventions
control group:Pseudo-transcutaneous electrical acupoint stimulation
Sponsors
the First Affiliated Hospital of Wenzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: (1) Patients who have a clear diagnosis and require unilateral pterygium excision. (2) Aged 18 to 85 years. (3) Those with normal comprehension and communication skills. (4) Those who voluntarily join and sign the informed consent form.
Exclusion criteria
Exclusion criteria: (1) Localized skin infections. (2) Severe cardiovascular disease, severe lung, liver and kidney disease, etc. (3) Surgery lasting more than 3 hours. (4) Persons with mental illness or language communication and comprehension problems. (5) Long-term use of sedative and analgesic drugs. (6) Patients who have participated in other clinical trials within the last four weeks.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative quality of recovery score, QoR-40; | — |
Secondary
| Measure | Time frame |
|---|---|
| Numerical rating scale,NRS;State-trait anxiety inventory, STAI;Ramsay Sadation Scale,RSS; | — |
Countries
China
Contacts
Public ContactYunchang Mo
the First Affiliated Hospital of Wenzhou Medical University, Nanbaixiang Street, Ouhai District, Wenzhou, Zhejiang province, China
Outcome results
None listed