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Effect of pretreatment with transcutaneous electric acupoint stimulation on the quality of recovery after ambulatory colonoscopy

Effect of pretreatment with transcutaneous electric acupoint stimulation on the quality of recovery after ambulatory colonoscopy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15005774
Enrollment
Unknown
Registered
2015-01-04
Start date
2015-01-05
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

abdominal pain

Interventions

control:Patients receive sham TEAS before colonoscopy
TEAS:Patients receive TEAS pretreatment before colonoscopy

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Outpatients aged 18 to 65, ASA physical status I or II, asymptomatic, who scheduled for ambulatory colonoscopy diagnosis or treatment under general anesthesia, and provided voluntary informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: Patients with history of narcotic analgesic abuse, prior use of transcutaneous electric acupoint stimulator or acupuncture related treatment within 8 hours, injury or infection on either side of the spinal column below the inferior angle of scapula, cognitive impairments or communication barriers, pregnancy and emergency.

Design outcomes

Primary

MeasureTime frame
Incidence of abdominal pain;Intensity of abdominal pain measured by visual analogue scale;

Secondary

MeasureTime frame
Incidence of vomitting;Incidence of nausea;Incidence of abdominal distension;Duration of recovery room stay;Patient satisfaction scores;Acceptance to colonoscopy;

Countries

China

Contacts

Public ContactYanqing Chen
sxd605@163.com+86 13314935073

Outcome results

None listed

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