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Propofol based ansethesia and acupuncture for postoperative nausea and vomiting and early recovery quality in patients undergoing thyroidectomy:A Randomized,Controlled,2×2 Factorial Trial

Propofol based ansethesia and acupuncture for postoperative nausea and vomiting and early recovery quality in patients undergoing thyroidectomy:A Randomized,Controlled,2×2 Factorial Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082127
Enrollment
Unknown
Registered
2024-03-21
Start date
2024-03-22
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Thyroidectomy

Interventions

Sevoflurane anesthesia + postoperative sham acupuncture treatment group:General anesthesia was maintained by sevoflurane + remifentanil, and sham acupuncture was performed after surgery
Sevoflurane anesthesia + postoperative acupuncture treatment group:General anesthesia was maintained by sevoflurane + remifentanil, and acupuncture was performed after surgery
Propofol anesthesia + postoperative sham acupuncture treatment group:General anesthesia was maintained with propofol and remifentanil, and sham acupuncture was performed after surgery
Propofol anesthesia + postoperative acupuncture treatment group:General anesthesia was maintained with propofol + remifentanil, and acupuncture was performed after surgery

Sponsors

The Fourth Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Selected patients who underwent elective thyroidectomy in our hospital; 2) American Society of Anesthesiologists (ASA) grade I to III; 3) Age 18-80 years old, body mass index (BMI) 18-30kg /m²; 4) Agree to participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1) Infection or rupture at acupuncture points; 2) Patients with cervical spondylosis, motion sickness, and insufficient cerebral blood supply; 3) Patients with severe insufficiency of heart, liver, lung and kidney function; 4) Patients with immune system, blood system diseases and coagulation dysfunction.

Design outcomes

Primary

MeasureTime frame
Nausea and vomiting 24 hours after surgery;Headache and dizziness 24 hours after surgery;Early postoperative recovery quality;

Secondary

MeasureTime frame
Postoperative sleep quality;Pharyngalgia;

Countries

China

Contacts

Public ContactHuaqin Liu

The Fourth Hospital of Hebei Medical University

liuhuaqin@hebmu.edu.cn+86 135 8212 6106

Outcome results

None listed

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