Clinical Study on Electroacupuncture Intervention of Pain after Shoulder Arthroscopic Surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300068773

Enrollment

Unknown

Registered

2023-02-28

Start date

2023-03-01

Completion date

Unknown

Last updated

2023-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperativepain after Shoulder Arthroscopic Surgery

Interventions

Treatment group:electroacupuncture+PCA(contained normal saline )

Control group: sham electroacupuncture+PCA(contained analgesics)

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.admitted for shoulder arthroscopic surgery due to rotator cuff injury 2.aged from 18 to 65years old 3.American Society of Anesthesiologists(ASA)=?

Exclusion criteria

Exclusion criteria: 1.refuse to general anesthesia or patients with high risk of general anesthesia 2.suffered from pain caused by other disease were on chronic opioid therapy 3.inable to cooperate to long-term follow-up investigation or complete questionnaire

Design outcomes

Secondary

Measure	Time frame
dosage of analgesics at 24h after surgery;Inflammatory factor levels:PCT, CRP, TNF -a, IL-6, IL-8, IL-4 and IL-10;EEG;Nocturnal pain;postoperative nausea and vomiting, PONV;Athens Insomnia Scale, AIS;Patients' satisfaction;American Shoulder and Elbow Surgeon,ASEA;3D-CAM;Postoperative complications;	—

Primary

Measure	Time frame
Numerical Rating Scale(NRS);	—

Countries

China

Contacts

Public ContactNi liya

Changhai Hospital of Shanghai

onlyliuzs0@163.com13621740319

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026