effect of Dexmedetomidine and Neostigmine in ?patients with chronic back pai
Not Applicable
Recruiting
- Conditions
- chronic back pain.Low back pain
- Registration Number
- IRCT2016112620258N18
- Lead Sponsor
- Ethics committee in Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 33
Inclusion Criteria
Lumbar epidural block; 30-70 years; ASA I and II; lack of vitamin D
Exclusion criteria: Allergy for this drug; failure in epidural block; history of fracture; lack of psychological disorders
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Heart rate. Timepoint: every 5 minutes to recovery. Method of measurement: beat per minute.;Oxygen saturation. Timepoint: every 5 minutes to recovery. Method of measurement: percent.;Mean arterial pressure. Timepoint: every 5 minutes to recovery. Method of measurement: millimeter Hg.;Duration of analgesia. Timepoint: in recovery, one month and three months after block. Method of measurement: minute.;Pain. Timepoint: in recovery, one month and three months after block. Method of measurement: analog visual scale.
- Secondary Outcome Measures
Name Time Method