Health Condition 1: G978- Other intraoperative and postprocedural complications and disorders of nervous system Health Condition 2: J958- Other intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified Health Condition 3: I978- Other intraoperative and postprocedural complications and disorders of the circulatory system, not elsewhere classified
Conditions
Interventions
None listed
Sponsors
AIIMS Jodhpur
Eligibility
Inclusion criteria
Inclusion criteria: Patients who will be admitted to the ICU and receiving propofol sedation on mechanical ventilation will be included in the study.
Exclusion criteria
Exclusion criteria: 1. Patient care giver refusal or inability to give consent. 2. Patients on Neuromuscular Blocking drugs. 3. Patients being administered sedative drugs other than the prescribed regimens. 4. Patients having a history of stroke, coma, or head injury or any neurological impairment. 5. Patients with hypothermia (core temperature 6. Patients with haemodynamic instability(Mean BP 7. Patients with an APACHE II score of 15 or more on admission. 8. Patients with primary hyperlipidemia 9. Patients with pancreatitis 10. Patients with a Known allergy to eggs or propofol at the time of enrolment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess correlation of qCON with clinical sedation score, Richmond Agitation Sedation Score (RASS).Timepoint: At the time of completion of study | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome is to assess the ability of qCON to differentiate between inadequate, adequate and excessive sedation.Timepoint: At the time of completion of study | — |
Countries
India
Contacts
Public ContactHarsha Makam
AIIMS Jodhpur
Outcome results
None listed