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Monitoring end-tidal sevoflurane concentration for preventing awareness during anesthesia, a prospective clinical trial

Monitoring end-tidal sevoflurane concentration for preventing awareness during anesthesia, a prospective clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16008923
Enrollment
Unknown
Registered
2016-07-27
Start date
2011-01-01
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

Required endoscopic surgery disease?undergoing general anaesthesia

Interventions

Routine care group,Rcg:end-tidal sevoflurane concentration group
end-tidal sevoflurane concentration group:monitored with end-tidal sevoflurane concentration

Sponsors

Fujian Medical University Union Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: elective general anesthesia, endoscopy surgery, aged 18-80 years, normal hearing, language communication unobstructed, ASA I - III level, including liver laparoscopic gastrointestinal tract endoscopy surgery, urology department cavity, thoracic cavity mirror and gynecological laparoscopic surgery.

Exclusion criteria

Exclusion criteria: Hearing impairment, language communication difficulties (including, but not speak mandarin), is not willing to accept the follow-up, brain diseases (such as psychoneurosis, cerebral infarction, etc.).

Design outcomes

Primary

MeasureTime frame
the incidence of awareness of patients undergoing general anaesthesia;

Secondary

MeasureTime frame
the time of tracheal extubation;

Countries

China

Contacts

Public ContactJiebo Wang

Department of Anesthesiology, Fujian Medical University Union Hospital

258960368@qq.com+86 15959004325

Outcome results

None listed

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