Skip to content

Comparison between Sevoflurane (Inhalational Anesthetic) and Propofol (Intravenous Anesthetic) for their effects on recovery from Anesthesia in patients undergoing day care surgery

Time course of psychomotor, cognitive and ambulatory recovery after Sevoflurane day case Anesthesia: A randomized double blind study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/11/003153
Enrollment
100
Registered
2012-11-27
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: null- Undergoing elective day care surgical procedures

Interventions

Intervention1: Sevoflurane: The drug is an anesthetic drug which is routinely used in Operating Theatres. It is administered via inhalational route through an endotracheal tube following induction of

Sponsors

JIPMER Puducherry
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I/II patients undergoing elective day care surgical/gynecologic procedures of less than 1 hour duration

Exclusion criteria

Exclusion criteria: Patients with clinically significant cardiovascular, respiratory, hepatic, renal, allergic history, psychological and neurological disorders

Design outcomes

Primary

MeasureTime frame
1. Recovery of cognitive function from Anesthesia as assessed by time to response to painful stimuli, eye opening, obeying commands and recalling address 2. Recovery of ambulatory function after anesthesia as assessed by time to sitting up with and without support, standing with and without support, walking with and without support and climbing stairs. 3. Recovery of psychomotor function as assessed by Digit Symbol Substitution Test and Trieger Dot TestTimepoint: Assessments will be done 15 mins, 30 mins, 1 hour, 2 hours and 4 hours after switching off anesthetic agent nitrous oxide.

Secondary

MeasureTime frame
Incidence of side effects in each groupTimepoint: At 15 mins, 30 mins, 1 hour, 2 hours, 3 hours and 4 hours post-recovery

Countries

India

Contacts

Public ContactDr Satyen Parida

JIPMER Puducherry

jipmersatyen@gmail.com9940973502

Outcome results

None listed

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