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A clinical trial to evaluate the outcomes in terms of neurocognitive functions with the use of two most commonly used anaesthetic agents Isoflurane and Desflurane

Isoflurane And Desflurane For Postanaesthesia Neurocognitive Dysfunction (ID-PANCOD) - ID-PANCOD

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/10/006245
Enrollment
200
Registered
2015-10-12
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- Effects of Isoflurane and Desflurane on Cognitive Dysfunction following anaesthesia

Interventions

Intervention1: Desflurane: Relatively newer inhalational anaesthetic agent now being increasingly used for neurosurgeries due to its properties of rapid emergence. Many studies have demonstrated neuro

Sponsors

Post Graduate Institute of Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients scheduled for minimally invasive surgery under general anaesthesia Age between 18-65 years American Society of Anaesthesiologists (ASA) Grade I and II patients Patients with Glasgow Coma Scale (GCS) of 15

Exclusion criteria

Exclusion criteria: Cardiorespiratory disorders Associated cerebral disease Psychiatric illness Preoperative cognitive disorders Electrolyte and hormonal imbalance Second operation. Low level of education History of drug abuse Postoperative meningitis Administration of high dose steroids

Design outcomes

Secondary

MeasureTime frame
The secondary outcome variables will be a) Cognitive function at three months following anaesthesia b) Estimation of serological biomarkers of cognitive dysfunction. Timepoint: Cognitive function 1) At three months postoperative Estimation of serological biomarkers 1)preoperative 2) postoperative after one hour following anaesthesia 3) postoperative at one week

Primary

MeasureTime frame
The primary outcome variable will be assessment of cognitive function at one week following anaesthesia. The cognitive functions will be assessed preoperatively and compared with cognitive functions at one week following anaesthesia.Timepoint: Psychological tests for evaluating cognitive functions 1)preoperative 2) postoperative at one week

Countries

India

Contacts

Public ContactDr Hemant Bhagat

Post Graduate Institute of Medical Education and Research

hembhagat@rediffmail.com7087009529

Outcome results

None listed

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