Skip to content

Effect of anesthesia information before surgery in neurosurgical patients.

Role of Preoperative Anesthesia Counselling in the neursurgical patients: a randomized controlled open label study.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043327
Enrollment
50
Registered
2022-06-17
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: G969- Disorder of central nervous system, unspecified

Interventions

Intervention1: ANESTHESIA COUNSELLING: Patients will be allocated to the AC group, apart from surgical counselling that will receive preoperative anesthesia counselling. For anesthesia counselling, th

Sponsors

AIIMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adult patients [18-65 years] undergoing 2-3 level thoracolumbar spinal fusion surgery 2. Written informed consent 3. American Society of Anesthesiologists class I&II 4. Age of >18 years 5. Either gender 6. Spine pathologies undergoing 2-3 level thoracolumbar spinal fusion surgery 7. Full Glasgow coma score (E4V5M6) 8. Estimated operative time of

Exclusion criteria

Exclusion criteria: 1. Non consenting patient 2. Mini-Mental State Examination [MMSE] 3. Any history of previous brain surgery 4. Current or past history of any cardiac disease or medication 5. Any history of lung disease, liver or kidney dysfunction 6. Body mass index of > 35 kg/m2 7. Preoperative cognitive dysfunction

Design outcomes

Primary

MeasureTime frame
1.Time to emergence [from discontinuation of anesthetics to eye opening on command in minutes] 2.Extubation time [from discontinuation of anesthetics to tracheal extubation in minutes] Timepoint: At the end of surgery.

Secondary

MeasureTime frame
1. Postoperative delirium [assessed using CAM-ICU]Timepoint: 60 minutes after extubation;2. Postoperative early cognitive dysfunction [assessed using MMSE]Timepoint: 60 minutes after extubation;3. Patients satisfaction score [6-point Likert scale with a score ranging from 0 to 5]Timepoint: 60 minutes after extubation

Countries

India

Contacts

Public Contactindu kapoor

AIIMS NEW DELHI

dr.indu.me@gmail.com09013439134

Outcome results

None listed

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