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Clinical application of S-ketamine injection in patients with painless bronchoscopy

Clinical application of S-ketamine injection in patients with painless bronchoscopy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048444
Enrollment
Unknown
Registered
2021-07-07
Start date
2020-06-01
Completion date
Unknown
Last updated
2022-03-21

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

Conditions

Painless bronchoscopy treatment

Interventions

Group B:Esketamine Injection
Group A:Propofol + remifentanil

Sponsors

People's Hospital of Honghuagang District, Zunyi City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients who need painless ultra-thin bronchoscopy combined with EBUS-GS examination, aged 18 to 70 years, ASA I to III patients; those who have signed an informed consent form voluntarily.

Exclusion criteria

Exclusion criteria: Patients with major organ dysfunction; patients with malignant tumors; patients with severe respiratory diseases or other major diseases of the system; patients with allergies to the drugs in this study; patients with mental retardation.

Design outcomes

Primary

MeasureTime frame
Incidence of severe cough;Average number of coughs;

Secondary

MeasureTime frame
signs of life;Propofol dosage;Time to loss of consciousness and time to recovery;The incidence of adverse reactions;

Countries

China

Contacts

Public ContactHuang qin

People's Hospital of Honghuagang District, Zunyi City

419476550@qq.com+86 18275617061

Outcome results

None listed

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