Health Condition 1: - Health Condition 2: R688- Other general symptoms and signs
Conditions
Interventions
None listed
Sponsors
Department Of Anaesthesiology And Critical Care JNMCH AMU ALIGARH UP INDIA
Eligibility
Inclusion criteria
Inclusion criteria: Patients who are not able to self report pain Patients whose expected length of stay in ICU >12 hours Mechanically ventilated patients
Exclusion criteria
Exclusion criteria: Presence of residual effects of neuromuscular blocking agents Conscious patients Deep coma, deep sedation Severe brain injury Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of the relationship between the BPS and CPOT in assessing pain in ventilated patients in ICUTimepoint: 24 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of sensitivity when both techniques combinedTimepoint: 20 weeks;Comparison of specificity and sensitivity of pain assessment between BPS and CPOT scalesTimepoint: 20 weeks;Comparison of the intensity of pain during non invasive procedures using BPS and CPOTTimepoint: 4 weeks , 8 weeks ,12 weeks , 16 weeks , 20 weeks;Relationship between physiological parameters with that of BPS and CPOTTimepoint: 4 weeks ,8 weeks ,12 weeks , 16 weeks , 20 weeks | — |
Countries
India
Contacts
Public ContactSyed Moied Ahmed
DEPARTMENT OF ANAESTHESIOLOGY& CRITICAL CARE,JNMCH, AMU,ALIGARH,U.P, INDIA, 202002
Outcome results
None listed