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Effect of transcutaneous electrical acupoint stimulation combined with dexmedetomidine on nausea and vomiting and gastrointestinal function in obese patients after laparoscopic sleeve gastrectomy

Effect of transcutaneous electrical acupoint stimulation combined with dexmedetomidine on nausea and vomiting and gastrointestinal function in obese patients after laparoscopic sleeve gastrectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071599
Enrollment
Unknown
Registered
2023-05-18
Start date
2023-05-22
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Postoperative nausea and vomiting in patients undergoing elective laparoscopic sleeve gastrectomy

Interventions

Con:Continuous intravenous infusion of 0.9% normal saline
Dex:Continuous intravenous infusion of dexmedetomidine
TEAS:Intervention with the transcutaneous electrical acupoint stimulation at Neiguan point (PC6) and Zusanli point (ST36)
TEAS+Dex:Intervention with the TEAS at Neiguan and Zusanli point combined with Continuous intravenous infusion of dexmedetomidine

Sponsors

Capital Medical University, Beijing Shijitan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1 Age 16-65 years old; 2 ASA Grade I to III; 3 Voluntary informed consent

Exclusion criteria

Exclusion criteria: 1 transcutaneous electrical acupoint stimulation is contraindicated, including local skin damage, infection or electrophysiological devices implanted in the body; 2 Communication disorders, unable to cooperate with researchers; 3 Patients with myocardial infarction or cerebral infarction within half a year and patients with heart failure within 1 month; 4 long-term use of hormones or antiemetic drugs; 5 Patients with slow ventricular rate, sick sinus syndrome and preexcitation syndrome; 6 Patients with degree II and above atrioventricular block; 7 those who have taken opioids in the last 3 months; 8 Liver and kidney insufficiency; 9 Participants in other clinical trials within 3 months prior to study enrollment; 10 Other situations that researchers deem unsuitable for inclusion..

Design outcomes

Primary

MeasureTime frame
Postoperative nausea and vomiting;

Secondary

MeasureTime frame
Postoperative nausea and vomiting;Postoperative pain score; Perioperative sufentanil, remifentanil dosage;Serum Serum motilin, serotonin levels;Postoperative complications;

Countries

China

Contacts

Public ContactPengfei Liu

Capital Medical University, Beijing Shijitan Hospital

sfflpf@126.com+86 152 1062 6257

Outcome results

None listed

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