Health Condition 1: Y33- Other specified events, undetermined intent
Conditions
Interventions
Intervention1: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
Bhaktivedanta Hospital and Research Institute
All India Institute of Medical Sciences
King George Medical University
Eligibility
Inclusion criteria
Inclusion criteria: All genders Age 18 years or older Coma survivors CPR patients Cardiac arrest survivors
Exclusion criteria
Exclusion criteria: Subject on antipsychotic, anti-anxiety medications or taking treatment for any psychological condition prior to NDE, Patients who give a history of any underlying psychiatric condition, Medications that have, hallucination as an adverse event
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To analyse the common characteristics of Near-Death Experience subjects and its frequency experienced among the traumatic subjects. Timepoint: At the timepoint of 48 hours post regaining consciousness and at the timepoint of 6 month post the event of Near Death Experience (NDE) | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the impact of NDE on quality of life.Timepoint: At the timepoint of 6 month post the event of Near Death Experience (NDE) | — |
Countries
India
Contacts
Public ContactDr Komal Dalal
Bhaktivedanta Hospital and Research Institute
Outcome results
None listed