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This is a study to check the effect of blood flow to the brain after increase in blood pressure when using a drug called Dexmedetomidine in patients with brain tumours.

Effect of Dexmedetomidine infusion on static autoregulation of cerebral blood flow in patients with intracranial tumours

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/02/006680
Enrollment
20
Registered
2016-02-25
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- patients with intracranial tumour and patients posted for spinal cord procedures (no intracranial pathology)

Interventions

Intervention1: Dexmedetomidine: Dexmedetomidine (1 microgram/Kg) will be given over 10 minutes to patients without intracranial tumours ( spine surgeries) and static autoregulation will be assessed Co

Sponsors

Sri Chitra Tirunal Institute for Medical Science and Technology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Two groups of patients will be included (10 patients in each group) • Group I â?? patient with unilateral supra tentorial tumours • Group II â?? patients with no intra cranial pathology (lumbar spinal cord procedures) Inclusion criteria: •Patients categorized as American society of Anesthesiology (ASA) class 1 and 2. •Age 18-40 years. •Glasgow coma scale 15. •patients with unilateral tumour in supratentorial compartment like glioma and meningioma (GroupI) •Patients posted for lumbar spinal cord procedures including laminectomy, discectomy and spinal cord tumour excision (Group II)

Exclusion criteria

Exclusion criteria: • Patient refusal • American society of Anesthesiology (ASA) class III and above • Age less than 18 years and more than 40 years. • Emergency surgery • Presence of intracranial vascular abnormalities ( Aneurysm, Arterio venous malformation) • Known allergy to Dexmedetomidine or any α2 agonists. • Known allergy to Inj. Phenylephrine • Preoperative heart rate • Systemic hypertension stage III & above • Antihypertensive medication with α-methyldopa or Clonidine. • Patient on beta blockers • Presence of Coronary artery disease, Left ventricular dysfunction, • Pregnant or Nursing woman. • Abnormal temporal bone window for transcranial Doppler insonation • Difficulty in localizing intracranial vasculature by Transcranial color Doppler • Participation in another drug study during the preceding 1 month period.

Design outcomes

Primary

MeasureTime frame
static cerebral vascular autoregulationTimepoint: 1. Baseline and 2.After administration of Dexmedetomidine (10 minutes after baseline)

Secondary

MeasureTime frame
mean flow velocity of middle cerebral artery and Pulsatility index, cerebral perfusion pressure derived from flow velocity data.Timepoint: 1. baseline 2.after dexmedetomine (1mcg/kg over 10 minutes)

Countries

India

Contacts

Public ContactARULVELAN

Sri Chitra Tirunal Institute for Medical Science and Technology

drarulvelan@gmail.com9048842282

Outcome results

None listed

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