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Prevention of postoperative nausea and vomiting in patients undergoing laparoscopic sleeve gastrectomy with spontaneous electric intradermal needle (P6) compared with conventional intradermal needle: a prospective, randomized, controlled study

Prevention of postoperative nausea and vomiting in patients undergoing laparoscopic sleeve gastrectomy with spontaneous electric intradermal needle (P6) compared with conventional intradermal needle: a prospective, randomized, controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053533
Enrollment
Unknown
Registered
2021-11-24
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-10-04

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

Conditions

None listed

Interventions

Sponsors

The Fifth People's Hospital of Chengdu
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Aged 20-50 years, BMI 35-49.9kg/m^2, ASA I-III grade. 2. Patients who intend to undergo laparoscopic sleeve gastrectomy and agree to participate in the experiment.

Exclusion criteria

Exclusion criteria: 1. Those who have nausea or vomiting before surgery and apply antiemetics; 2. Long-term use of sedative and analgesic drugs or alcohol abusers; 3. Mental disorder, unable to communicate normally, with a history of epilepsy, still taking anti-epileptic drugs; 4. Poorly controlled diabetes (fasting blood sugar greater than 12mmol/L), hypertension (more than 180/110mmHg); 5. Bleeding disease, abnormal coagulation function and menstrual period; 6. Serious systemic diseases (heart disease, coronary heart disease, pacemaker).

Design outcomes

Primary

MeasureTime frame
Incidence of nausea and vomiting within 48 hours after surgery;

Secondary

MeasureTime frame
The operation time;Anesthesia time;Intraoperative opioid dosage;Nausea, vomiting and retching symptom assessment (INVR) scale score;The frequency and dosage of anti-emetic rescue were recorded 0-48h after operation;The number and dosage of rescue analgesia were recorded from 0 to 48 hours after operation;

Countries

China

Contacts

Public ContactZeng Min

The Fifth People's Hospital of Chengdu

910050140@qq.com+86 18328309015

Outcome results

None listed

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