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Effect of different anesthesia depth on postoperative nausea and vomiting in female patients with unilateral radical thyroid cancer resection: a single-center, single-blind, randomized clinical trial

Effect of different anesthesia depth on postoperative nausea and vomiting in female patients with unilateral radical thyroid cancer resection: a single-center, single-blind, randomized clinical trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083260
Enrollment
Unknown
Registered
2024-04-19
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

postoperative nausea and vomiting

Interventions

experimental group :The sevoflurane drug dose was adjusted to maintain bispectral index range of 40-45
Control group:The sevoflurane drug dose was adjusted to maintain bispectral index range of 55-60

Sponsors

Qilu Hospital, Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Female patients diagnosed with thyroid cancer; (2) Age: 18-65 years old; (3) BMI:18-30kg/m2; (4) American Association of Anesthesiologists (American Society of Anesthesiologists, ASA) grade I-II; (5) Patients who plan to have unilateral radical resection of thyroid cancer surgery under general anesthesia.

Exclusion criteria

Exclusion criteria: (1) Patients with preoperative history of motion sickness or PONV; (2) Patients with gastrointestinal diseases, craniocerebral diseases, oogenic diseases that can cause nausea and vomiting or have received chemotherapy in the past few weeks; (3) Taking antiemetic drugs in the ward within 24 hours before surgery; (4) Patients with serious neurological and mental diseases; (5) Severe heart, lung, cerebrovascular, or liver and kidney function damage; (6) Do not agree to participate in this study.

Design outcomes

Primary

MeasureTime frame
The incidence of PONV at 24 hours after surgery;

Secondary

MeasureTime frame
The incidence of PONV at other postoperative time points;The use of remedial antiemetic medication at various time points;visual analogue scale, VAS;Use of intraoperative cardiovascular active drugs;Time of awakening;Time of extubation;The occurrence of respiratory depression, hypotension, bradycardia and chills;

Countries

China

Contacts

Public ContactFeng Qi

Qilu Hospital, Shandong University

qifeng66321@sina.com+86 185 6008 3756

Outcome results

None listed

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