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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01023763
Other study ID # 2009/1584a
Secondary ID
Status Completed
Phase Phase 2
First received December 1, 2009
Last updated May 12, 2016
Start date November 2009
Est. completion date December 2012

Study information

Verified date May 2016
Source University of Oslo
Contact n/a
Is FDA regulated No
Health authority Norway: Data Protection AuthorityNorway: Ministry of Health and Care ServicesNorway:National Committee for Medical and Health Research Ethics
Study type Interventional

Clinical Trial Summary

The primary objective for the project is to evaluate whether nursing home residents who require intravenous fluids and intravenous antibiotics, can be treated just as well or even better in the nursing home as in the hospital. In Vestfold, Norway, a structured training program in the intravenous treatment of dehydration and infections in nursing homes is planned. The 3IV study will evaluate if this leads to an equal or better patient trajectory and reduced hospital admittance.


Description:

1. Can a structured training program in administration of intravenous fluids and antibiotics lead to a reduced number of admissions and days in hospitals among nursing home residents?

2. Can treatment with intravenous fluids or antibiotics in nursing homes provide an equally good or better patient trajectory compared to patients hospitalized for the same treatment? We will look at duration of symptoms, direct and indirect complications, and mortality rates.

3. Can treatment costs for the public health service be reduced when patients are treated with intravenous fluids and /or antibiotics in the nursing home instead of being admitted to the hospital?

4. Can treatment for dehydration and infections in the nursing home rather than in a hospital provide an equally or better satisfaction in patients, next of kin and staff?

5. How are difficult ethical issues handeld by medical staff at the nursing homes and the hospital when nursing home patients receive intravenous treatment?


Recruitment information / eligibility

Status Completed
Enrollment 330
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Nursing home residents in need of intravenous fluids or antibiotics

Exclusion Criteria:

- Patients who needs hospitalization due to either co-morbidity or seriousness of disease

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
A structured training program
A structured training program in nursing homes in the intravenous treatment of dehydration and infections.

Locations

Country Name City State
Norway University of Oslo Oslo

Sponsors (1)

Lead Sponsor Collaborator
University of Oslo

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary All cause morbidity and mortality Within 30 days after disease onset Yes
Secondary Number of admissions and days in hospitals among nursing home residents Primarily within 30 days after disease onset Yes
Secondary Patient trajectory Primarily within 30 days after disease onset Yes
Secondary Satisfaction in patients, next of kin and staff Primarily within 30 days after disease onset Yes
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