Effects of transcutaneous electrical acupoint stimulation on recovery quality of patients after Pterygium excisio

Phase 1

• Conditions: Pterygium

• Registration Number: ITMCTR2200005572
• Lead Sponsor: the First Affiliated Hospital of Wenzhou Medical University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: Not specified

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

(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.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative quality of recovery score, QoR-40;

Secondary Outcome Measures

Name	Time	Method
umerical rating scale,NRS;State-trait anxiety inventory, STAI;Ramsay Sadation Scale,RSS;