FindTrial
Sign In

To Compare The Dose Of Propofol Drug For Induction Of General Anaesthesia As Determined By Entropy Monitoring Against The Standard Induction Dose In Elderly Patients

To Compare The Dose Of Propofol For Induction Of General Anaesthesia As Determined By Entropy Monitoring Against The Standard Induction Dose In Elderly Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/048808
Enrollment
94
Registered
2023-01-09
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Giving propofol based on entropy monitoring and standard dose -: Control group will be given based on standard dose ,based on weight .Entropy group will be given propofol based on entro

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients in age group more than 50 years of either sex belonging to American Society of Anesthesiologist 1&2

Exclusion criteria

Exclusion criteria: 1.Patients who have history of allergy to propfol.2.patients with history of cardiac disease.3.ASA 3 and ASA 4 STATUS patients.4.long term use of drugs affecting the central nervous system.

Design outcomes

Primary

MeasureTime frame
To know whether there is decrease in requirements of propofol during induction of general Anesthesia in elderly patients.Timepoint: 4 weeks—

Secondary

MeasureTime frame
To know the haemodynamic stability of the patientsTimepoint: To record systolic Blood pressure,diastolic blood pressure,mean blood pressure,heart rate at baseline,after induction.after intubation at 1 minute.—

Countries

India

Contacts

Public ContactMadhavi Buddhi

Seth G.S.Medical College & KEM Hospital

madhavi_70@yahoo.com9969105307

Outcome results

None listed

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