transcutaneous acupoint electrical stimulation methods for postoperative pain management after surgical abortion

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IPR-15007145

Enrollment

Unknown

Registered

2015-09-25

Start date

2013-08-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

surgical abortion

Interventions

the preoperative:TEAS

postoperative:TEAS

combination:TEAS

local anesthesia:lidocaine

TEA control:TAE+lidocaine

blank control:NONE

Eligibility

Sex/Gender

Female

Age

18 Years to 31 Years

Inclusion criteria

Inclusion criteria: Aged 18–40 years, gestational period between 7 to 12 weeks, andconfirmed pregnant by an ultrasonography examination were enrolled in this study.

Exclusion criteria

Exclusion criteria: The subjects were excluded if they reported an allergy to propofol, sufentanil, or TEAS; they had used opioid medications in the previous month; their operation duration was greater than 10 min; andthey suffered from inflammatory disease or psychiatric illness.

Design outcomes

Primary

Measure	Time frame
pain score;	—

Countries

China

Contacts

Public ContactXie Wen-xia

17396352@qq.com+86 13868653068

Outcome results

None listed

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