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Critical IllnessNCT04755374

Clinical Characteristics and Discharge Assessment of Patients From Palliative Care

An observational study of Critical Illness, run by Diskapi Yildirim Beyazit Education and Research Hospital at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The number of people having chronic diseases and the demand for palliative care has increased. The factors that have an impact on length of stay and discharge of patient who were admitted to palliative care center will be investigated. Read more about this study

Who is it for?
Ages 18 to 100 years
Conditions the study is for
Critical Illness
What is being tested?
Discharged ≤ 21 days and Prolonged discharge
How many people
103 participants
Where
1 siteTurkey (Türkiye)
Study dates
20 Feb 2021to 20 Apr 2021
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 100 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients with a critical ilness/conditions

Who may be able to join

  • Adult patients admitted to the palliative care unit

Who cannot join

  • Patients not consenting to participate the study

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Diskapi Yildirim Beyazit Teaching and Research Hospital

    Ankara

Other trials in Turkey (Türkiye)

About this study

Official title: Clinical Characteristics and Discharge Assessment of Patients in a Recent Founded Palliative Care Unit

The number of people having chronic diseases and the demand for palliative care has increased. The factors that have an impact on length of stay and discharge of patient who were admitted to palliative care center will be investigated.

Read the detailed description

Adult patients admitted to the Diskapi Yildirim Beyazit Teaching and Research Hospitals Palliative Care Unit between August 2018 and September 2020 and discharged to their home will be retrospectively evaluated.

Patient's age, gender, diagnosis, conditions/comorbidities, Karnofsky Performance Scale, discharge status (death, intensive care unit or at home), gastrostomy status, presence of tracheostomy and/or mechanical ventilation, nutritional status (total parenteral nutrition or enteral nutrition), pressure ulcers, the lowest and highest recorded hemoglobin concentration, white blood cell count and serum sodium concentration and the education level of the patient and the caregiver will be recorded. Patients will be grouped according to length of stay (LOS) as Group 1: discharged in equal or less than 21 days or Group 2: Prolonged discharged in longer than 21 days and analysed accordingly

Being tested
Discharged ≤ 21 days, Prolonged discharge
Keywords
Critical illness, Palliative care, Length of stay
Medical subject headings
Critical Illness

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Discharged ≤ 21 daysOther

    Discharged from palliative care unit in equal less than 21 days

  • Prolonged dischargeOther

    Discharged from palliative care unit in longer than 21 days

Study groups in NCT04755374
Study groupRoleWhat they receive
Group 1Discharged from palliative care unit in equal or less than 21 days
Receives: Other: Discharged ≤ 21 days
Group 2: Prolonged discharged in longer than 21 daysDischarged from palliative care unit in longer than 21 days
Receives: Other: Prolonged discharge

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Length of stay

    Length of stay will be determined after discharge

    Measured: 24 hours after discharge

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Feb 2021
  2. Study start20 Feb 2021
  3. Primary completion20 Mar 2021
  4. Study completion20 Apr 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Retrospective
Enrolment
103 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04755374
Sponsor's protocol ID
Palliative-Discharge
Status last verified
Feb 2021
First submitted
11 Feb 2021
Last updated
14 Jul 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Gomes B, Higginson IJ. Where people die (1974--2030): past trends, future projections and implications for care. Palliat Med. 2008 Jan;22(1):33-41. doi: 10.1177/0269216307084606.

    PubMed 18216075
  • Lau F, Downing GM, Lesperance M, Shaw J, Kuziemsky C. Use of Palliative Performance Scale in end-of-life prognostication. J Palliat Med. 2006 Oct;9(5):1066-75. doi: 10.1089/jpm.2006.9.1066.

    PubMed 17040144
  • Kelly A, Conell-Price J, Covinsky K, Cenzer IS, Chang A, Boscardin WJ, Smith AK. Length of stay for older adults residing in nursing homes at the end of life. J Am Geriatr Soc. 2010 Sep;58(9):1701-6. doi: 10.1111/j.1532-5415.2010.03005.x. Epub 2010 Aug 24.

    PubMed 20738438

Questions about this trial

What is this clinical trial studying?

An observational study of Critical Illness, run by Diskapi Yildirim Beyazit Education and Research Hospital at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 14 Jul 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Length of stay (time frame: 24 hours after discharge). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04755374, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jul 2021.

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