Effect of wrist-ankle acupuncture on propofol dose in painless bronchoscopy: a randomized, controlled, double-blind trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000034207

Enrollment

Unknown

Registered

2020-06-28

Start date

2020-07-01

Completion date

Unknown

Last updated

2020-06-29

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

Conditions

Painless bronchoscopy

Interventions

Experimental group:wrist-ankle acupuncture

Control Group:False needle

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients who agree to accept painless bronchoscopy; 2. ASA I-III patients; 3. Patients aged 18-70 years, male and female are not limited.

Exclusion criteria

Exclusion criteria: 1. Patients undergoing emergency painless bronchoscopy; 2. The object of language communication or mental disorder; 3. Patients with acute attack of asthma or acute upper respiratory tract infection; 4. Patients with severe cardiopulmonary disease (LVEF < 30%) before operation; 5. Propofol hydrochloride injection allergic history of patients; 6. Preoperative use of potential neuromodulatory drugs (diazepam, etc.); 7. Patients who were examined for more than 20 minutes.

Design outcomes

Secondary

Measure	Time frame
The incidence of hypoxemia;Incidence of cough;vital signs;	—

Primary

Measure	Time frame
Propofol dosage;	—

Countries

China

Contacts

Public ContactHao Wei

Hebei Hospital of traditional Chinese Medicine

hao_wei800@163.com+86 13832122359

Outcome results

None listed

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