The Effect of Reduced Dose of Enoxaparin on the Outcomes of Treatment With Enoxaparin

This study is currently recruiting participants. (see Contacts and Locations)
Verified June 2011 by Hadassah Medical Organization
Information provided by:
Hadassah Medical Organization Identifier:
First received: July 19, 2006
Last updated: July 3, 2011
Last verified: June 2011

We hypothesize that reduced dose of enoxaparin in elderly patients will result in reduced proportion of patients with therapeutic anti Xa activity and reduced clinical efficacy.

Acute Coronary Syndrome
Venous Thromboembolism
Atrial Fibrillation

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: The Effect of Reduced Dose of Enoxaparin on the Laboratory and Clinical Outcomes of Treatment With Enoxaparin

Resource links provided by NLM:

Further study details as provided by Hadassah Medical Organization:

Estimated Enrollment: 500
Study Start Date: July 2006
Estimated Study Completion Date: October 2015
Detailed Description:

Patients treated with enoxaparin will be followed, sociodemographic , clinical and laboratory data will be collected. Clinical efficacy as well as adverse events will be monitored.


Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

patients admitted to tertiary hospital


Inclusion Criteria:

  • treatment with enoxaparin

Exclusion Criteria:

  • no
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00354796

Contact: Mordechai Muszkat, MD 00-972-2-6776449

Hadassah Medical Organization Recruiting
Jerusalem, Israel, 91120
Contact: Arik Tzukert, DMD    00 972 2 6776095   
Contact: hadas Lemberg, PhD    00 972 2 6777572   
Principal Investigator: Mordechai Muszkat, MD         
Sponsors and Collaborators
Hadassah Medical Organization
Principal Investigator: Mordechai Muszkat, MD Hadassah University Hospital
  More Information

No publications provided

Responsible Party: Mordechai Muszkat, Hadassah University Hospital Identifier: NCT00354796     History of Changes
Other Study ID Numbers: enoxap-HMO-CTIL
Study First Received: July 19, 2006
Last Updated: July 3, 2011
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Hadassah Medical Organization:

Additional relevant MeSH terms:
Acute Coronary Syndrome
Venous Thromboembolism
Venous Thrombosis
Angina Pectoris
Cardiovascular Diseases
Chest Pain
Embolism and Thrombosis
Heart Diseases
Myocardial Ischemia
Signs and Symptoms
Vascular Diseases processed this record on March 26, 2015