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Effect of cranial electrical stimulation on postoperative fatigue in women undergoing caesarean section: a randomized sham controlled study

Effect of cranial electrical stimulation on postoperative fatigue in women undergoing caesarean section: a randomized sham controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045140
Enrollment
Unknown
Registered
2021-04-07
Start date
2021-04-01
Completion date
Unknown
Last updated
2021-11-08

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

Conditions

perioperative fatigue during cesarean delivery

Interventions

Sponsors

Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1.Selective cesarean delivery, ASA class II ~ III; 2.Combined spinal and epidural anesthesia; 3.The gestational age is 38 to 42 weeks, and the fetal heart rate is good.

Exclusion criteria

Exclusion criteria: 1. Less than 18 years old or more than 45 years old; 2. The head basin does not weigh, fetal growth disorder; 3. Medical and delivery diseases, serious hypertension, diabetes, cardiovascular and cerebrovascular diseases, and major surgery history; 4. Have CES use experience, skin damage in CES application area; 5. 10 cases of contraindications to the use of electrical stimulation: patients using implantable electronic devices (such as cardiac pacemakers); Patients with intracranial metal implants; Patients with fever, electrolyte disturbance or unstable vital signs; Patients with local skin injury or inflammation; Patients with bleeding tendency; Patients with increased intracranial pressure; Patients with acute massive cerebral infarction; Patients with epilepsy and taking epileptic drugs; Patients with implanted devices with metal components in the treatment area; Patients with hyperalgesia in the stimulated area; 6. Have mental illness; Or a history of surgery for major traumatic brain injury; 7. Unable to understand or refuse to sign the informed consent.

Design outcomes

Primary

MeasureTime frame
Fatigue scale score;

Countries

China

Contacts

Public ContactCao Junli

The Affiliated Hospital of Xuzhou Medical University

Caojljl0310@163.com+86 15162160809

Outcome results

None listed

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