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The Effect of Acupuncture Therapy at the Buccal Region on the Incidence of Nausea and Vomiting in Post Cesarean Section Patients Receiving Intrathecal Morphine Analgesia: A Randomized Controlled Trial

The Effect of Acupuncture Therapy at the Buccal Region on the Incidence of Nausea and Vomiting in Post Cesarean Section Patients Receiving Intrathecal Morphine Analgesia: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000052
Enrollment
Unknown
Registered
2026-01-10
Start date
2026-01-31
Completion date
Unknown
Last updated
2026-02-02

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

Buccal Acupuncture Group:Select Upper Jiao Point, Middle Jiao Point, Lower Jiao Point, Lumbar Point and Sacral Point (bilaterally)
use disposable sterile buccal needles (specification: 0.16×13mm), and after routine disinfection of the local skin at the acupoints, perform rapid needle insertion with a depth of approximately 2-3mm
after Deqi is achieved, apply gentle lifting-thrusting and twirling manipulation at a frequency of about 60-80 times per minute for 1-2 minutes, then retain the needle for 30 minutes
the buccal acupuncture therapy is performed at three time points: 30 minutes after fetal umbilical cord clamping (the first time), 9:00 AM on the first postoperative day (the second time), and 9:00 AM
Control Group:No special treatment.

Sponsors

Northern Theater General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 45 years old; 2. Nulliparas or multiparas; 3. Gestational age of 37 to 42 weeks; 4. Singleton pregnancy; 5. American Society of Anesthesiologists Physical Status Classification II-III; 6. Scheduled for cesarean section under subarachnoid anesthesia

Exclusion criteria

Exclusion criteria: 1. Allergy to morphine, local anesthetics and other drugs involved in the study; 2. With severe hepatic and renal dysfunction, cardiovascular diseases, endocrine system diseases, etc.; 3. Facial skin infections, lesions or skin diseases, making them unsuitable for buccal acupuncture manipulation; 4. History of mental illness or cognitive impairment, unable to cooperate with pain assessment and relevant questionnaires; 5. Preoperative comorbidity of motion sickness, or use of antiemetics, analgesics or other drugs that may affect the study results within 24 hours before surgery.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative nausea and vomiting;

Secondary

MeasureTime frame
Number of postoperative nausea and vomiting episodes;Severity of postoperative nausea and vomiting;Incidence of postoperative pruritus;Severity of postoperative pruritus;Severity of postoperative resting pain;Severity of postoperative moving pain;Incidence of urinary retention;Time to first postoperative flatus;Time to first colostrum secretion;Postoperative plasma C-reactive protein (CRP) level;Postoperative plasma interleukin-6 level;Postoperative plasma tumor necrosis factor-a level;Postoperative cortisol level;Postoperative ß-endorphin level;Severity of postoperative anxiety and depression;Postoperative sleep quality;Postoperative quality of recovery;

Countries

China

Contacts

Public ContactYuan Zhenru

People's Liberation Army (PLA) Northern Theater Command General Hospital

359996356@qq.com13998271403

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 7, 2026