"Iatrogenesis Imperfecta"- Extent and Characteristic in NICU in Israel.
This study has been completed.
Sponsor:
Bnai Zion Medical Center
Information provided by:
Bnai Zion Medical Center
ClinicalTrials.gov Identifier:
NCT00264563
First received: December 12, 2005
Last updated: June 16, 2011
Last verified: August 2005
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Purpose
Iatrogenesis is inevitable in the NICUs.
| Condition | Intervention | Phase |
|---|---|---|
|
Iatrogenesis in NICU |
Behavioral: Increasing the level of awareness to Iatrogenesis Behavioral: Increasing awareness . |
Phase 1 |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
Further study details as provided by Bnai Zion Medical Center:
| Estimated Enrollment: | 750 |
| Study Start Date: | November 2005 |
| Estimated Study Completion Date: | April 2006 |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
Behavioral
The intervention is basically by letting the care givers to be aware that there is active recording of iatrogenesis
|
Behavioral: Increasing the level of awareness to Iatrogenesis
Increasing the level of awareness to Iatrogenesis
Behavioral: Increasing awareness .
Increasing awareness to Iatrogenesis and active daily recordings
Other Name: In the first 3 months the medical teams were unaware of recordings while in next 3 months they became aware to recordings
|
Detailed Description:
In the first 3 months of the study we will document Iatrogenic events in 3 NICUs in Israel without informing the medical and nursing staff. In the second 3 months of the study we will try to draw the attention of the medical and nursing staff that we are documenting iatogenesis, and we will assess wether this intervention will decrease the events of Iatrogenesis.
Eligibility| Ages Eligible for Study: | up to 6 Months |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Ifants admitted to NICU during the study period
Criteria
Inclusion Criteria:All infants in NICU -
Exclusion Criteria:None
-
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00264563
Locations
| Israel | |
| Bnai Zion Medical Center | |
| Haifa, Israel | |
| Bnai Zion Medical Center, Rambam Medical Center, Barzilay Medical Center | |
| Haifa ans Ashkelon, Israel, 31048 | |
Sponsors and Collaborators
Bnai Zion Medical Center
Investigators
| Principal Investigator: | Amir Kugelman | Senior Neonatologist |
More Information
No publications provided
| Responsible Party: | Amir Kugelman, Bnai Zion Medical Center |
| ClinicalTrials.gov Identifier: | NCT00264563 History of Changes |
| Other Study ID Numbers: | 80/05 |
| Study First Received: | December 12, 2005 |
| Last Updated: | June 16, 2011 |
| Health Authority: | Israel: Ministry of Health United States: Food and Drug Administration |
ClinicalTrials.gov processed this record on June 18, 2013