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SMART Pilot study

SMartPilot guided Anesthesia and Recovery Trial (SMART): A Pilot study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001786
Enrollment
Unknown
Registered
2011-12-12
Start date
2011-12-01
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

surgery patients

Interventions

A:SMART Pilot anesthesia advisory system iii. Duration of the intervention During surgery/anesthesia
B:Anesthesia administration guided by using the SMART Pilot advisory system or routine care based on hemodynamic changes

Sponsors

The Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. mentally capable to consent; 2. to receive general anesthesia >= 2 hours; 3. ASA 1-3.

Exclusion criteria

Exclusion criteria: 1. Surgery that include wake up test; 2. Patient with history of drug or alcohol abuse or chronic use of hypnotics or opioid; 3. Patient with history of allergy to anesthetic drugs.

Design outcomes

Primary

MeasureTime frame
Rate of change in Quality of recovery score in postoperative interviews and at 30 days after surgery;

Secondary

MeasureTime frame
1. Incidence of postoperative complications;2. Patient satisfaction;3. Analgesic and anesthetic consumption;4. Pain score in the postoperative period;

Countries

China

Contacts

Public ContactMatthew Chan
mtvcahn@cuhk.edu.hk+852 26322736

Outcome results

None listed

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