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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00192816
Other study ID # 2038CTIL
Secondary ID
Status Recruiting
Phase N/A
First received September 13, 2005
Last updated September 13, 2005
Start date June 2005

Study information

Verified date September 2005
Source Rambam Health Care Campus
Contact Maria Nassar, Doctor
Phone 0502061707
Email mashers@netvision.net.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine response to pain in Alzheimer's disease.We plan to study the effect of diffuse noxious inhibitory controls(counterirritation phenomenon)and the autonomic nervous system reaction(reflected by the heart rate) in Alzheimer's disease. The study's hypothesis is that pain perception and autonomic nervous system reaction are altered in Alzheimer's disease.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 55 Years to 95 Years
Eligibility Inclusion Criteria:

- Clinical diagnosis of Alzheimer's disease Must be able to understand a simple pain scale

Exclusion Criteria:

Neuropathy Psychotropic drugs use -

Study Design

Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Intervention

Behavioral:
reaction to pain


Locations

Country Name City State
Israel Neurocognitive unit,Neurophysiology laborator Rambam Health Care Campus Haifa

Sponsors (1)

Lead Sponsor Collaborator
Rambam Health Care Campus

Country where clinical trial is conducted

Israel,