FindTrial
Sign In

The impact of Bis-target anaesthetic depth on pediatric patient outcome after scoliosis surgery

A prospective, randomised clinical trial of two levels of anaesthetic depth on pediatric patient outcome after scoliosis surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016359
Enrollment
Unknown
Registered
2018-05-28
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-06-05

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

Conditions

Scoliosis

Interventions

Low BIS:Keep BIS value between 40 to 50
High BIS:Keep BIS value between 50 to 60

Sponsors

Beijing Children's Hospital, National Center for Children's Health, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 14 Years

Inclusion criteria

Inclusion criteria: Age 2 to 14 years, ASA physical status 2 or 3, surgery expected to last =2 hours, post-operative hospital stay expected to be =7 nights, general anesthesia, able to monitor BIS throughout anaesthesia.

Exclusion criteria

Exclusion criteria: Unable to monitor BIS, medication history of sedative hypnotic drugs, analgesic and/or antipsychotics epilepsy, other nerve system diseases and/or psychiatric disorders with poor control, unable to consent.

Design outcomes

Primary

MeasureTime frame
Inpatient all cause mortality;—

Secondary

MeasureTime frame
Major complications;BIS value;Extubation time;Anesthetic dosage;MAP;Hospital stay;ICU stay;Cost;—

Countries

China

Contacts

Public ContactJIANMIN ZHANG

Beijing Children's Hospital, National Center for Children's Health, Capital Medical University

zjm428@sina.com+86 13910299602

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026