FindTrial
Sign In

The effect of intraoperative Transcutanclus Electrical Acupoint Stimulation on hyperalgesia and pain after caesarean section

The effect of intraoperative Transcutanclus Electrical Acupoint Stimulation on hyperalgesia and pain after caesarean section

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005830
Enrollment
Unknown
Registered
2022-04-09
Start date
2022-04-09
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Postoperative pain

Interventions

TEAS group:Transcutanclus Electrical Acupoint Stimulation
Control group:Blank intervention

Sponsors

Linshui County People's Hospital, Guangan, Sichuan
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. 18 to 45 years old; 2. ASA I-?; 3. Caesarean section under intraspinal anesthesia; 4. Voluntarily to receive patient-controlled intravenous analgesia; 5. Voluntarily to participate the study.

Exclusion criteria

Exclusion criteria: 1. With chornic pain or receiving analgesic drugs within three months; 2. With damage or rash on skin of study loctation; 3. With temporary cardiac pacemaker; 4. Can not cooperate with the study because of any reason.

Design outcomes

Primary

MeasureTime frame
Mechanical pain sensitivity;—

Secondary

MeasureTime frame
Postoperative pain score;Analgesic requirements;—

Countries

China

Contacts

Public ContactGuangyou Duan
duangy@hospital.cqmu.edu.cn18323376014

Outcome results

None listed

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