Skip to content

Comparing 2 different ratios of ketamine and propofol on patient vitals while giving anesthesia in abdominal surgeries

Comparison of ketamine to propofol in 1:2 versus 1:4 ketofol admixture on peri-intubation hemodynamics in exploratory laparotomy:a randomised comparative double blind clinical trial - nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067027
Enrollment
90
Registered
2024-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: R00-R99- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified

Interventions

Intervention1: Group B :1:4 Ketofol Group: Group B admixture will contain 25mg of ketamine and 100mg propofol diluted up to 20 ml in a single syringe In the OT, vital monitors will be attached and bas

Sponsors

UCMS and GTB Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Consenting patients aged 18-65 years posted for expolrative laparotomy under general anaesthesia 2)Hemodynamically stable patients

Exclusion criteria

Exclusion criteria: 1)Patient with heart block on peri operative ECG 2)Patient with heart rate less than 50bpm 3)Hemodynamically unstable patient with mean arterial pressure less than 60mmHg 4)Patient on inotropes 5)Patient with signs and symptoms of raised intracranial tension 6)Patient with known allergy to any of the drug used

Design outcomes

Primary

MeasureTime frame
To assess and compare incidence of hypotension between groups A and BTimepoint: Baseline 0 minute

Secondary

MeasureTime frame
1) HR, SBP, DBP immediately post induction, 2) HR, SBP, DBP immediately post intubation, 3) Consumption of norepinephrine till 1 hour post intubation, 4) Intubating conditions during intubation 5) HR and MAP at the end of 5 minutes, 10 minutes 15 minutes, 20 minutes, 30 minutes and 1 hour, Timepoint: 1)post induction 2)at the time of intubation 3)post intubation 4)5,10,15,20,30,60 minutes post intubation.

Countries

India

Contacts

Public ContactDr Suhani Agarwal

UCMS and GTB Hospital

rudoc@rediffmail.com9560678023

Outcome results

None listed

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