Desflurane sparing effect of propofol and dexmedetomidine :A randomized study

A comparative study on fixed dose Dexmedetomidine and Propofol infusions on desflurane consumption during BIS guided laparoscopic surgeries A randomized controlled study

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/08/020485

Enrollment

Registered

2019-08-01

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: K807- Calculus of gallbladder and bile duct without cholecystitis

Interventions

Intervention1: Desflurane sparing effect of Propofol and Dexmedetomidine: A fixed dose of Dexmedetomidine and Propofol infusion ON Desflurane consumption during BIS guided laparoscopic surgeries Con

Eligibility

Inclusion criteria

Inclusion criteria: Elective laparoscopic surgeries ASA I and II

Exclusion criteria

Exclusion criteria: Patients allergic or contraindications to study drugs ASA III and above Pregnant and lactating women

Design outcomes

Primary

Measure	Time frame
Desflurane consumption Timepoint: Time to achieve Ramsay sedation score of 2, Time to reach modified Aldrete score of 9 post extubation and time taken for first analgesic request	—

Secondary

Measure	Time frame
PAIN ASSESMENT AND SEDATION SCORE ASSESMENTTimepoint: FROM POST EXTUBATION 1]TIME TO FIRST ANALGESIC REQUEST[mins] 2]TIME TAKEN TO REACH RAMSAY SEDATION SCORE OF 2[mins] 3]TIME TAKEN TO REACH MODIFIED ALDRETE SCORE OF 9[mins]	—

Countries

India

Contacts

Public ContactDr Kishore M

Sri Venkateswara Institute of Medical Sciences

hemanthn1973@gmail.com9493547658

Outcome results

None listed

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