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Correlation of patients hippocampal volume with recovery time after sedation in MRI unit

Not Applicable
Conditions
Health Condition 1: G96- Other disorders of central nervoussystem
Registration Number
CTRI/2021/07/034647
Lead Sponsor
ational Institute of Mental Health and Neurosciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All patients who need sedation to undergo brain MRI, aged between 5 and 60 years.

Patients who will require both spine and brain MRI (with spine pathology).

Patients receiving sedation for 20 to 60 minutes duration. 

Exclusion Criteria

Refusal to provide informed consent

Patients with identified causes of delayed waking up like hypothyroidism, hyponatremia Na ( <135 mEq/L) [3], hypernatremia Na >145 mEq/L [9], hypo/hyperglycemia, hypothermia with axillary temperature < 350C. 

Patients with known liver and/or renal dysfunction. (Defined as elevated or aspartate amino-transferase/ alanine amino-transferase > 5 times [10] when reports are available, serum creatinine >1.2 mg/dL) [11]

Patients on inotropic support.

Patients who are intubated.

Patients with motor component of Glasgow Coma Scale (GCS) <= 5 and eye component < 4 Patients diagnosed with intracranial space occupying lesions.

Patients post intracranial surgeries/ resection surgeries.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Assessment of recovery is made without any stimulation (tactile or noxious). Time to spontaneous eye opening and limb movement by the patients will be recorded from the time of stoppage of infusion. <br/ ><br>The hippocampal volume will be calculated bilaterally in pre-contrast-volumetric MPRAGE sequence of brain imaging by the radiologist using Statistical Parametric Mapping. Timepoint: 0, 5, 7, 9�.. minutes from the stoppage of infusion ( i.e., 5 minutes after stoppage of the infusion, and every 2 minutes up to a point where the patient becomes fit for discharge )
Secondary Outcome Measures
NameTimeMethod
assessment of adequacy to discharge will be assessed as per the Modified Aldrete Score which tests the activity level at request.Timepoint: 0, 5, 7, 9â?¦.. minutes from the stoppage of infusion ( i.e., 5 minutes after stoppage of the infusion, and every 2 minutes up to a point where the patient becomes fit for discharge )
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