Clinical Trials Logo

Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01851486
Other study ID # 0393-12-RMB.CTIL
Secondary ID
Status Withdrawn
Phase N/A
First received May 2, 2013
Last updated October 1, 2017
Start date January 2013
Est. completion date September 2016

Study information

Verified date October 2017
Source Rambam Health Care Campus
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The role of alpha2 receptor agonist on pain perception and modulation will be examined. In addition whether this is mediated through the opioid system will be examined. Pain perception and modulation will be examined before and after administration of Clonidine or placebo together with Naloxone or saline.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date September 2016
Est. primary completion date September 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Healthy volunteers

- Age 18-40

- No chronic disease

Exclusion Criteria:

- Subjects who suffer from chronic pain / pain syndrome

- use of anti-depressant or anti-psychotic drugs

- suffering from cardiovascular disease

- breast feeding

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Clonidine
Clonidine 0.15 mg
Naloxone
naloxone 0.15 mg/kg
placebo

Other:
saline


Locations

Country Name City State
Israel Rambam Health Care Campus Haifa

Sponsors (1)

Lead Sponsor Collaborator
Rambam Health Care Campus

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary The changes in pain responses after administration of alpha 2 agonist and mu receptor antagonist The change in pain perception (pain thresholds and pain ratings of suprathresholds stimuli) and in the excitatory and inhibitory pain modulation responses (assessed by the temporal summation and conditioned pain modulation paradigms) will be examined before and after administration of alpha 2 agonist with and without mu receptor antagonist 2 years