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Comparitive study of dosage of propofol in patients receiving Midazolam versus Dexmedetomidine during conscious sedation in Colonoscopic procedure

A Comparison of the dose requirement of Propofol in patients receiving Midazolam versus Dexmedetomidine during Conscious Sedation in Colonoscopic procedures

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/04/024896
Enrollment
80
Registered
2020-04-28
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: K529- Noninfective gastroenteritis and colitis, unspecified

Interventions

None listed

Sponsors

Kasturba Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA Physical status 1 & 2

Exclusion criteria

Exclusion criteria: 1.Age less than 20 years and more than 60 years 2.ASA Physical status 3 & 4 3.Allergy to any one of the drugs like Midazolam,Opioids,Dexmedetomidine and egg 4.History of drug abuse like Alcohol,Tobacco,opioids and benzodiazepine 5.Sleep apnea 6.Patient refusal and uncooperative ondividuals not available to give an informed consent. 7.History of colonic or rectal surgery

Design outcomes

Primary

MeasureTime frame
1. To compare the effects of dexmedetomidine versus midazolam administered as premedicants and their effects on total propofol requirements, peri-procedural hemodynamics, sedation and pain reliefTimepoint: July 2020

Secondary

MeasureTime frame
1. Compare the effects of dexmedetomidine versus midazolam on periprocedural hemodynamic change,Level of sedation,assessment of pain,total requirement of propofol,recovery using modified aldrete score, Patient Satisfaction score by Numeric rating scale Endoscopist Satisfaction by Verbal rating scale Timepoint: july2020

Countries

India

Contacts

Public ContactDr Bejoy Abraham

Kasturba Medical College,Mangalore

Madhusudan.upadya@manipal.edu984522340

Outcome results

None listed

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