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The variation of bis during inhalation anesthesia

The variation of bis during inhalation anesthesia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-17011005
Enrollment
Unknown
Registered
2017-03-28
Start date
2017-03-24
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

urological disease

Interventions

observation group:inhalation anesthesia

Sponsors

Shanghai Children's Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients ASA I or II, scheduled for elective urological surgery

Exclusion criteria

Exclusion criteria: Patients suffering from neurological disorders, treatment with antiepileptic or stimulants, preexisting lung or cardiac disease, airway abnormalities.

Design outcomes

Primary

MeasureTime frame
bis;

Secondary

MeasureTime frame
Preoperative general condition;intraoperative vital signs;adverse effects;

Countries

China

Contacts

Public ContactYing Sun

Shanghai Children's Medical Center

yingsun821@163.com+86 13621738118

Outcome results

None listed

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