The effect of chamomile Essense on Cesarean post operative pain relief
Not Applicable
- Conditions
- pain.Acute pain
- Registration Number
- IRCT2016042427558N1
- Lead Sponsor
- Sabzevar University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 128
Inclusion Criteria
Consent for participation in the study; Ability to speake Farsi
The same type of anesthesia (spinal anesthesia) and anesthetic used; 38 to 42 weeks of gestational age; Nulli parous.
exclusion criteria:Reluctance to continue participating in the exercises; Use powerful hypnotics or analgesics drugs; Having allergy and breathing problems; History of warfarin
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain Intensity. Timepoint: befor of aromatherapy and after 20 minute. Method of measurement: Visual Analog Scale.
- Secondary Outcome Measures
Name Time Method Pain Quality. Timepoint: befor of aromatherapy and after 20 minute. Method of measurement: Modify Short Form McGill Pain Questionnaire.