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Clinical observation of acupuncture on optimizing intraoperative anesthesia to improve postoperative PONV in patients with benign breast tumor resection

Clinical observation of acupuncture on optimizing intraoperative anesthesia to improve postoperative PONV in patients with benign breast tumor resection

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068703
Enrollment
Unknown
Registered
2023-02-27
Start date
2023-02-27
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Post-operative nausea and vomiting

Interventions

Control group:Conventional breast surgery treatment
Acupuncture anesthesia group:Preoperative and intraoperative electroacupuncture treatment
sham-acupuncture anesthesia group:Preoperative and intraoperative sham- electroacupuncture treatment

Sponsors

Yueyang Hospital of Integrative Traditional Chinese Medicine and Western Medicine, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with benign breast tumor. 2.ASA (American Society of Anesthesiologists) classification I to III, elective proposed breast surgery under general anesthesia. 3.age = 18 years and = 70 years, female. 4.understood, agreed to participate in this study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.patients with serious heart, respiratory, liver or kidney diseases. 2.skin allergy, severe breakage or infection at the needle site. 3.dry heaving, vomiting or moderate to severe nausea, or chronic nausea or vomiting 24 h prior to anesthesia. 4.having received antiemetic treatment within 5 days prior to surgery. 5.those who require daily opioid use for any reason within 7 days prior to surgery. 6.those who are unable to cooperate with mental disorders, impaired consciousness, behavioral disorders, etc. 7.those who are expected to require placement of a gastric tube.

Design outcomes

Primary

MeasureTime frame
Sufentanil dosage;Blood pressure;Heart rate;Oxygen saturation level;Anesthesia time;Surgery time;Resuscitation time;Incidence of nausea and vomiting at different time periods;Severity of nausea and vomiting at different times of the day;Additional postoperative doses of metoclopramide;

Secondary

MeasureTime frame
age;Height;weight;PONV Risk Score;current perception threshold;pain equivalent current;

Countries

China

Contacts

Public ContactLiJing

Yueyang Hospital of Integrative Traditional Chinese Medicine and Western Medicine, Shanghai University of Traditional Chinese Medicine

1971921250@qq.com18930568565

Outcome results

None listed

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