A randomized controlled study for acupoint stimulation using subacupuncture to relieve postoperative nausea and vomiting in patients undergoing gynecological and obstetrical surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900026709

Enrollment

Unknown

Registered

2019-10-19

Start date

2019-11-01

Completion date

Unknown

Last updated

2019-10-21

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

Conditions

Nausea and vomiting

Interventions

experimental group:Earring hole press needle

control group:none

Eligibility

Sex/Gender

Female

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who planned gynecological surgery and cesarean section; 2. Non-smoker; 3. Patients with a history of motion sickness; 4. Opioid patients; 5, Aged > 18 years and < 65 years; 6, ASA class I - II.

Exclusion criteria

Exclusion criteria: 1. Patients who refuse acupoint stimulation; 2. Patients with antiemetic drugs; 3. Patients with dexamethasone; 4, mental disorders, unable to communicate with patients; 5. Allergic to adhesive tape and hypodermic acupuncture.

Design outcomes

Primary

Measure	Time frame
Incidence of nausea and vomiting;	—

Countries

China

Contacts

Public ContactWei Hao

Hebei Hospital of Traditional Chinese Medicine

zhang6620072@163.com+86 13832122359

Outcome results

None listed

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