Skip to content

Analgesia by Single or Dual Acupoints Stimulation After Radical Mastectomy

Effect of Combined-acupoint or Single-acupoint Stimulation Before Surgery on Post Mastectomy Pain: a Multicentre Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02741726
Acronym
ASDAS
Enrollment
593
Registered
2016-04-18
Start date
2016-05-25
Completion date
2018-10-23
Last updated
2019-10-16

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

Conditions

Pain

Brief summary

The purpose of this study is to compare the effects of dual acupoints and single acupoint transcutaneous electrical acupoint stimulation (TEAS) pretreatment on incidence of Post-Mastectomy Pain Syndrome(PMPS) in patients undergoing operation of breast cancer.

Detailed description

Patients were randomly assigned to three groups, receiving 30min TEAS before anesthesia respectively. The acupoints of dual point group are bilateral Neiguan points(PC6) combined with Danzhong point(RN17), single point group is bilateral Neiguan points(PC6), and the false stimulation group only attach electrodes without electric current. The frequency of TEAS is set to 2/15 Hz. Intraoperative anesthetic dosage of propofol and remifentanil was recorded. Three and six months after surgery, follow-up about chronic pain was made by telephone or face-to-face using the follow-up questionnaire. The adverse events were recorded.

Interventions

Electric stimulation was given through electrode attached to acupoints

patients were only attached electrodes without electric current

Sponsors

Zhihong LU
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Scheduled for operation of breast cancer; * ASA(American Society of Anesthesiologists)I-II; * Aged between 18 and 65; * Informed consented。

Exclusion criteria

* Suffered from the contraindication of TEAS including the local skin breakage, infection or planted with the electrophysiology device; * Unable to communicate and coordinate with the researcher, such as suffering from language comprehension deficits or mental diseases; * Certain/suspicious addiction with alcohol, analgesics or other drugs; * Unstable Angina or myocardial infarction occurred in 3 months; NYHA(New York Heart Association) is 3 or higher; * Blood pressure ≥ 180/110 mm Hg while preoperative visiting; * Suffered from diabetic complications including diabetic ketoacidosis, hyperosmolar coma, infection, macroangiopathy, diabetic nephropathy, retinopathy, cardiomyopathy, neuropathy and diabetic foot; * Severe dysfunction of liver or kidney meaning one of ALT(Alanine Transaminase), AST(Aspartate Transaminase), ALP(alkaline phosphatase) or TBIL(total bilirubin) is 2 times higher that normal or creatinine clearance \< 30 ml/min or serum creatinine \> 177umol/L; * Participate in the other clinical trial 3 month before the enrollment.

Design outcomes

Primary

MeasureTime frame
Incidence of chronic pain six months after surgerysix months after surgery

Secondary

MeasureTime frame
Remifentanil consumption during the surgeryfrom start of surgery to end of surgery, at an average of 2.5 hours
the time to the first verbal responseend of the anesthetics infusion to patient's first response to verbal command,on an average of 30 minutes
the time to extubationend of the anesthetics infusion to extubation,on an average of 30 minutes
postoperative nausea and vomiting within 24 h after surgeryend of surgery to 24 hours after surgery,on an average of 24 hours
respiratory depression within 24 hours after surgeryend of surgery to 24 hours after surgery,on an average of 24 hours
Incidence of chronic pain three months after surgerythree months after surgery
Visual Analogue Scale scores within 24 hours after surgeryend of surgery to 24 hours after surgery,on an average of 24 hours
demand of rescue analgesics within 24 hours after surgeryend of surgery to 24 hours after surgery,on an average of 24 hours
pain score at 3m after surgerythree months after surgery
pain score at 6m after surgerysix months after surgery
patients' s satisfaction scores on analgesia within 24 hours after surgeryend of surgery to 24 hours after surgery,on an average of 24 hours

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026