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Addition of lidocaine to prophylactic ondansetron and dexamethasone in adults at high risk for postoperative nausea and vomiting. A randomized, controlled, double-blind study

Addition of lidocaine to prophylactic ondansetron and dexamethasone in adults at high risk for postoperative nausea and vomiting. A randomized, controlled, double-blind study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072311
Enrollment
Unknown
Registered
2023-06-09
Start date
2023-06-10
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

Hysteromyoma

Interventions

A:Intravenous infusion of 0.3ug/kg sufentanil+1.5mg/kg lidocaine, and continuous pumping of 0.1ug/kg and 2mg/kg respectively until the end of the operation
B:Intravenous infusion of sufentanil 0.3ug/kg + normal saline, and continuous pumping of 0.1ug/kg + normal saline until the end of the operation

Sponsors

Yichang Central People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1):18-50; 2)ASA ? ?; 3)=180min; 4)BMI 14~35kg/m2.

Exclusion criteria

Exclusion criteria: 1) patients with a history of opioid allergy; 2) analgesic sedatives, antiemetics and anti-pruritus drugs were used 24 hours before surgery; 3) Patients with body temperature higher than 38°C or accompanied by symptoms of acute upper respiratory tract infection within 24 hours before surgery; 4) Patients with a history of bronchial asthma; 5) Patients diagnosed with moderate to severe sleep apnea syndrome before surgery; 6) Patients with difficult airway or previous history of abnormal anesthesia recovery with preoperative assessment; 7) Renal impairment (BUN and or Cr> upper limit of normal values); 8) Liver function impairment (ALT and or AST > 1.5 times the upper limit of normal); 9) Patients with a history of severe head trauma and intracranial hypertension within 6 months; 10) Patients with psychiatric or neurological diseases, or patients who cannot correctly express their wishes; 11) Patients with a history of long-term sedation and analgesic drugs or monoamine oxidase inhibitors; 12) Estimated blood loss during surgery is greater than 100ml; 13) Those who have participated in clinical trials of other drugs in the past month; 14) Patients who cannot undergo ASA or FLACC scoring for various reasons; 15) Patients with other conditions that the investigator considers unsuitable for inclusion. 16) Abnormal breath holding test. 17) Have not quit smoking within the past half month. 18) Patients with uncontrolled hypertension or those with arrhythmias.

Design outcomes

Primary

MeasureTime frame
Nausea and vomiting within 24 hours of surgery;Postoperative VAS score within 24 hours of surgery;

Secondary

MeasureTime frame
extubation time;Sedation score;exhaust time;Additional analgesic dose;24-hour QoR-40 score;Vasoactive drug consumption;

Countries

China

Contacts

Public ContactGong Yuan

Yichang Central People's Hospital

gy-yc@163.com+86 139 8674 6821

Outcome results

None listed

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