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Transcutaneous electric acupoint stimulation in flexible bronchoscopy

Transcutaneous electric acupoint stimulation in flexible bronchoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016612
Enrollment
Unknown
Registered
2018-06-12
Start date
2018-06-25
Completion date
Unknown
Last updated
2018-06-18

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

Conditions

Flexible bronchoscopy

Interventions

Group T:Transcutaneous electrical acupoint stimulation
Control group:Sham stimulation

Sponsors

Department of Anesthesiology, The Fourth Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing diagnostic elective flexible bronchoscopy; 2. Bronchoscopy for the first time; 3. Aged 18 to 70 years; 4. BMI 18.5 to 35; 5. ASA physical classification system status I-III.

Exclusion criteria

Exclusion criteria: 1. Emergency bronchoscopy; 2. Therapeutic bronchoscopy; 3. Endobronchial ultrasound; 4. Poor communication; 5. Patients with mental disease; 6. Pregnant and lactating women; 7. Patients with baseline oxygen desaturation(resting hypoxaemia,160mmHg or 100beats/min or <50beats/min,arrhythmia; 12. A patient who has had an TEAS treatment; 13. Patients taking part in other clinical studies; 14. Other reasons that are not suitable for the study.

Design outcomes

Primary

MeasureTime frame
cough score;

Countries

China

Contacts

Public ContactWei Zhang

Department of Anesthesiology, The Fourth Affiliated Hospital of Harbin Medical University

harbinzw2@163.com+86 13946006143

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 20, 2026