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To estimate the concentration of propofol achieved in brain during anesthesia using a software.

Estimation of effect site concentration of propofol using Tivatrainer software for target control infusion. An observational study. - TIVA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/03/012491
Enrollment
35
Registered
2018-03-12
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- ASA 1 and 2 patients coming for surgery.

Interventions

None listed

Sponsors

Institute Research Grant
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • ASA 1 & 2 • Elective surgery duration

Exclusion criteria

Exclusion criteria: 1. Patients with CNS disorders and head injury 2. Pregnant women 3. Allergy to administered drugs 4. Body mass index more than 25. 5. Difficult airway 6. Drug or alcohol abuse

Design outcomes

Primary

MeasureTime frame
Effect site concentration of propofol.Timepoint: During anesthesia.—

Secondary

MeasureTime frame
Entropy value, Time to peak effect, Awakening time, Time to open eyes to response, Total consumption of propofol.Timepoint: During anesthesia—

Countries

India

Contacts

Public ContactRAJKUMAR S

JIPMER

dr.lenin@gmail.com9487981140

Outcome results

None listed

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