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The effect of Tarooneh on pai

Phase 2
Conditions
lumbar pain.
Low back pain
Registration Number
IRCT2017063034815N1
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
70
Inclusion Criteria

Age range 30 to 50 years; Having discopathy without fusion; Not fasting; Does not have a disease that increases or decreases pain; Do not breast-feed or be pregnant;Non-addiction;Specific underlying disease, such as heart disease;Tarooneh insensitivity.
Exclusion criteria:Unwillingness to attend the study; Transfer to another department.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: One hour before the intervention and 7,13 and 25 hours after the intervention. Method of measurement: Visual Analog Scale(vas).
Secondary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: One hour before the intervention and 7,13 and 25 hours after the intervention. Method of measurement: Sphygmomanometer.;Temperature. Timepoint: One hour before the intervention and 7,13 and 25 hours after the intervention. Method of measurement: Centimeter using a thermometer.;Heart beat. Timepoint: One hour before the intervention and 7,13 and 25 hours after the intervention. Method of measurement: pulse/min using a Puls Oximeter.;Breathing. Timepoint: One hour before the intervention and 7,13 and 25 hours after the intervention. Method of measurement: respiratory rate/ min by viewing.
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