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Comparing the anaesthesia recovery quality using three different agents in patients undergoing lumbar laminectomy

Comparison of recovery profiles of patients undergoing lumbar laminectomy under propofol, sevoflurane or desflurane anesthesia. A randomized, prospective, clinical, comparative study - None

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/04/018478
Enrollment
75
Registered
2019-04-08
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: M519- Unspecified thoracic, thoracolumbar and lumbosacral intervertebral disc disorder

Interventions

Control Intervention1: Propofol, Sevoflurane and Desflurane: Comparing recovery profiles of patients undergoing surgery under propofol, sevoflurane or desflurane anaesthesia

Sponsors

SGPGI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA grade I and II 2. Age between 18 to 65 year 3. Patients of either gender 4. Education level minimum up to 8th standard 5. Single or two level disease necessitating decompression/discectomy without instrumentation

Exclusion criteria

Exclusion criteria: 1. Patient refusal 2. Inability to read or speak or communicate 3. Patients with psychiatric disorders/behavioral impairment or on antipsychotic drugs 4. Patients with significant hepatic, cardiovascular,pulmonary or renal disorders 5. Morbid obesity 6. Patients with allergy to study drugs or history of malignant hyperthermia 7. Chronic drug/alcohol abuse

Design outcomes

Primary

MeasureTime frame
1) To compare the preoperative versus postoperative cognitive and psychomotor recovery profiles of patients undergoing lumbar laminectomy and discectomy under general anaesthesia maintained with propofol, sevoflurane or desflurane.Timepoint: Thrice preoperatively. Post extubation at 15 minutes, 30 minutes, 1 hour, 2 hours, 3 hours and at 4 hours.

Secondary

MeasureTime frame
1) To compare the incidences of postoperative complications like headache, giddiness, nausea, vomiting or pain at injection sites. 2) To compare the time taken by subjects administered these three anaesthetic regimens to achieve a modified Aldreteâ??s Score of 9. 3) To compare the satisfaction of the patients regarding the quality of anaesthesia Timepoint: After 4 hours post intubation

Countries

India

Contacts

Public ContactDr Amit Kumar Verma

SGPGI, Lucknow

shashian2002@yahoo.co.in8004904594

Outcome results

None listed

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