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NCT03520023 Clinical Trial

Critical Care and Palliative Care Medicine Together in the ICU

Palliative Care Clinical Trial

Official title:
Does Early vs Usual Palliative Care Consultation Augment the Critical Care Physician to Decrease Healthcare Utilization and Increase Caregiver Satisfaction

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03520023
Other study ID # 18-001107
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 4, 2018
Est. completion date March 1, 2020

Study information
Verified date October 2020
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Will earlier palliative care medicine consultation in the ICU result in decreased length of stay in the ICU and hospital, as well as, increased patient and family satisfaction. Secondary questions to be answered is if this early consultation changes ICU and hospital death, discharge destinations, hospice admissions, code status changes, and withdrawal of life sustaining interventions.

Recruitment information / eligibility
Status Completed
Enrollment 95
Est. completion date March 1, 2020
Est. primary completion date March 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 1. Age >80 years 2. Apache II score >14 3. SOFA score > 9 4. Pre-existing functional dependency (admitted from ALF, SNF, LTAC, etc.) 5. Late stage dementia (bed-bound, nonverbal, incontinent, or unable to self-nourish/tube feed) 6. Stage 4 metastatic disease 7. Consideration to place permanent feeding tube or trach 8. Recurrent ICU admissions in the past year 9. Post-cardiac arrest 10. End-stage disease (lung, ESRD, ESLD) 11. ICU perceived need

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Palliative Care Consult
Consult of hospital palliative care service for those meeting study inclusion criteria

Locations
Country Name City State
United States Mayo Clinic in Florida Jacksonville Florida

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Patient satisfaction Measure will assessed by using the family satisfaction with care in the intensive care unit form (FS-ICU 24) 1 year
Secondary ICU length of stay 1 year
Secondary Ventilator Days 1 year
Secondary Percentage admission to hospice 1 year
See also
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