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The effect of percutaneous acupoint electrical stimulation relieving burn patients’ resting pain on intraoperative opioid dosage

The effect of percutaneous acupoint electrical stimulation relieving burn patients’ resting pain on intraoperative opioid dosage

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078615
Enrollment
Unknown
Registered
2023-12-14
Start date
2023-12-02
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Intraoperative opioid dosage

Interventions

Sponsors

The First Affiliated Hospital of Shihezi University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-60 years old, gender is not limited; (2) ASA grade I-II, no history of major systemic diseases; (3) Patients with moderate burns, i.e.11%-30% of second-degree burns or less than 10% of third-degree burns; (4) Burn scab grafting or debridement under general anesthesia; (5) Preoperative F-VAS score 30mm-60mm; (6) Able to cooperate with pain assessment and voluntarily sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with contraindications to percutaneous electrical stimulation of acupuncture points (such as arrhythmias such as arrhythmias such as the burn site covering the acupuncture points that need stimulation, installing a pacemaker, complicated with sinus syndrome, severe bradycardia (<50 beats/min) or more than second degree atrioventricular block); (2) Those with a history of chronic pain and long-term use of analgesic drugs before surgery; (3) recent use of antipsychotic drugs, alcoholism or drug abuse; (4) Pregnant or lactating patients; (5) Patients with a history of severe cardiovascular, liver and kidney diseases and cerebrovascular accidents.

Design outcomes

Primary

MeasureTime frame
Intraoperative opioid dosage;

Secondary

MeasureTime frame
Postoperative pain score;Incidence of postoperative adverse reactions;The amount of postoperative salvage analgesic used;Rate of pain improvement after electrical stimulation;

Countries

China

Contacts

Public ContactQian Liu

Shihezi University

1187517402@qq.com+86 137 6245 6720

Outcome results

None listed

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