Effects of total propofol or remifentanil anesthesia during 30 min before end of operation on the extubation parameters of patients undergoing radical mastectomy

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900025320

Enrollment

Unknown

Registered

2019-08-24

Start date

2019-09-01

Completion date

Unknown

Last updated

2019-08-27

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

Conditions

radical mastectomy

Interventions

Control group:total propofol anesthesia

Observe group:total sevoflurane anesthesia

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Aged 18 to 65 years, ASA I-II, Scheduled to have single side of radical mastectomy.

Exclusion criteria

Exclusion criteria: Plumonary dysfunction, contraindication to muscle relaxants, additive to alcohol and drugs, BMI>=26, allergy to soybean, and pregnant woman.

Design outcomes

Primary

Measure	Time frame
extubation parameters;	—

Secondary

Measure	Time frame
adverse outcome after extubation;	—

Countries

China

Contacts

Public ContactYan Ni

The First Affiliated Hospital of Nanjing Medcial University

niyan812@163.com+86 13913844476

Outcome results

None listed

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