Condition 1: Nausea. Condition 2: Vomiting. Nausea Vomiting
Conditions
Interventions
Intervention 1: Intervention group: : In intervention group the amount of 5 drops of chamomile extract are dripped in 10 ml of water with the dropper for each participant of the intervention group, ha
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 45 Years
Inclusion criteria
Inclusion criteria: Age between 20-45 Women who have their first childbirth Women who have the ability to determine the severity of nausea as directed Women who have nausea before intervention Women whose surgery is due to cesarean section
Exclusion criteria
Exclusion criteria: Women who have NG tubes Women who are allergic to herbal extracts Women with a history of obstructive pulmonary disease Women who have nausea due to a specific illness with a doctor's approval
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nausea score in Visual Analogue Scale. Timepoint: Evaluation of nausea within half an hour before intervention and 30 minutes and 4 hours after starting of using the extract of chamomile. Method of measurement: Visual Analogue Scale.;Vomiting number on the vomiting recording form. Timepoint: Check the number of vomiting within before intervention and 30 minutes and 4 hours after starting of using the extract of chamomile. Method of measurement: Recording form of vomiting number. | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety score on the Beck Anxiety Inventory. Timepoint: Anxiety assessment at the beginning of the intervention and 4 hours after starting of using the extract of chamomile. Method of measurement: Beck Anxiety Inventory. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBehnaz Hosseinzade
Hamedan University of Medical Sciences
Outcome results
None listed