Skip to content

To assesss whether Ketamine-Propofol can be replaced by Ketamine-Dexmedetomidine for sedation in surgical excision of breast fibroadenoma

A comparative study to assess the efficacy between Ketamine-Propofol and Ketamine-Dexmedetomidine on sedation in surgical excision of breast fibroadenoma - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073968
Enrollment
70
Registered
2024-09-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: N602- Fibroadenosis of breast

Interventions

Intervention1: KETAMINE - DEXMEDETOMIDINE: TO STUDY THE EFFICACY OF KETAMINE - DEXMEDETOMIDINE AS SEDATION IN CASES OF FIBROADENOMA KETAMINE AT THE DOSE OF 1-2mg/kg AND DEXMEDETOMIDINE AT THE DOSE OF

Sponsors

Gulbarga Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: adult patient aged from 18 yrs to 60 yrs posted for surgical excision of fibroadenoma and belongs to ASA-1 and ASA-2 those who have given consent

Exclusion criteria

Exclusion criteria: adult aged more than 60 years and anticipated difficult airway and those who have allergy to drugs pregnancy

Design outcomes

Primary

MeasureTime frame
to determine the efficacy between ketamine-propofol and dexmedetomidine- ketamine on adequate sedation using Ramsay sedation scaleTimepoint: Ketamine- Propofol is administered during the start of the surgery and using Ramsay sedation scale sedation score is given for every 5mins until the surgery is completed . For another group patient receiving Ketamine-Dexmedetomidine sedation score is given after this drug administration using Ramsay sedation scale from the start of the surgery to every 5 mins until the surgery is completed

Secondary

MeasureTime frame
recovery time from sedation in cases posted for surgical excision of breast fibroadenomaTimepoint: recovery time is assessed once the surgery is completed using modified Aldrete score is given every 5 mins upto 30 mins

Countries

India

Contacts

Public ContactDr Keerthana R

Gulbarga Institute of Medical Sciences

drrhatti@gmail.com9740478820

Outcome results

None listed

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