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Effect of drug given during spine surgery for old aged patients on Recovery and mentation

Effect of Intraoperative Dexmedetomidine infusion on Postopearative Cognitive Dysfunction and Recovery Quality in an Elderly Patient posted for Spine Surgery: a Randomized Prospective Double Blinded Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/026077
Enrollment
60
Registered
2020-06-23
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: O- Medical and Surgical

Interventions

Intervention1: Dexmedetomidine: dose - 0.5mcg/kg intravenous bolus , followed by 0.5mcg/kg/hour till the start of skin closure Control Intervention1: placebo: equal dose as compared to dexmedetomidine

Sponsors

Indraprastha Apollo Hospital New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with American Society of Anesthesiologists (ASA) physical status I-III aged 60- 80 years old, undergoing elective lumbar spine surgery

Exclusion criteria

Exclusion criteria: 1. Patients age less than 60 years and more than 80 years old. 2. Patients with a pre-operative or intraoperative ECG (electrocardiogram) that showed severe bradycardia (sinus rhythm, heart rate less than 50/ min) or conduction block 3. Patients with associated renal, hepatic and respiratory dysfunction. 4. Patients with history of central nervous system disease such as head injury, stroke, previous neurosurgery, behavioral disturbances or mental retardation. 5. Patients with preoperative cognitive dysfunction (MMSE 6. Patients on β-blockers, cimetidine, digoxin, α2-agonists, anticonvulsants or psychotropic medications 7. Patients with allergy to dexmedetomidine or another alpha-2 adrenergic receptor agonist

Design outcomes

Primary

MeasureTime frame
1. Mini- Mental State Examination (MMSE) Scores. 2. 15-item quality of recovery score (QoR15) questionnaire. Timepoint: 1. Before Anaesthesia 2. Day 1 of Surgery 3. Day 2 of Surgery 4. Day 3 of Surgery

Secondary

MeasureTime frame
1. Intraoperative propofol consumption. 2. Intraoperative and postoperative fentanyl requirement. 3. Haemodynamic changes Timepoint: till the duration of surgery

Countries

India

Contacts

Public ContactDr K J Choudhury

Indraprastha Apollo Hospital

kjchoudhury@samvedana.org

Outcome results

None listed

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