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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01844544
Other study ID # MMC130061-13CTIL
Secondary ID
Status Completed
Phase N/A
First received April 29, 2013
Last updated February 24, 2014
Start date June 2013
Est. completion date October 2013

Study information

Verified date February 2014
Source Meir Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Clalit Health Services
Study type Observational [Patient Registry]

Clinical Trial Summary

the purpose of the study is to:

1. Identify and characterize drug related problems in patients after a femur neck fracture that are hospitalized in the orthopedic department at "Meir" medical center.

2. Evaluate the contribution of a clinical pharmacist in identifying,characterizing and preventing drug related problems in patients after a femur neck fracture that are hospitalized in the orthopedic department at "Meir" medical center.


Recruitment information / eligibility

Status Completed
Enrollment 104
Est. completion date October 2013
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender Both
Age group 64 Years and older
Eligibility Inclusion Criteria:

- patients over 64

- patients after a femoral neck fracture

- patients hospitalized in the orthopedic ward at "Meir" medical center

- patients who speak Hebrew, Russian or English

Exclusion Criteria:

- patients under 64

- patients without a femoral neck fracture

- patients who don't speak Hebrew, Russian or English

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
inspection of medical records


Locations

Country Name City State
Israel Meir medical center Kfar - Saba

Sponsors (1)

Lead Sponsor Collaborator
Meir Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluate the overall number of drug related problems in patients with a femur neck fracture in the orthopedic department participants will be followed for the duration of hospital stay, an expected average of 7 days Yes
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