The severity of flatulence. Flatulence and related conditions
Conditions
Interventions
Intervention 1: Intervention group:40 drops of oral dill drop in 30 cc water in 3 times within 20 minutes after disconnecting serum and drinking tea. Intervention 2: Contol group:40 drops of placebo d
Treatment - Drugs
Placebo
Intervention group:40 drops of oral dill drop in 30 cc water in 3 times within 20 minutes after disconnecting serum and drinking tea.
Contol group:40 drops of placebo drop in 30 cc water in 3 times within 20 minutes after disconnecting serum and drinking tea.
Sponsors
Sabzevar University of Medical Science
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria:38-42 w pregnancy, single pregnancy, alive birth, transverse incision in cesarean, BMI:28-30, 18 -40 years old. Exclusion criteria: allergies to herbal combinations specially dill, differnce in type and volume for sedative and serum with other volunteers .
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The severity of flatulence. Timepoint: 3 times within 20 minutes and 120 minutes after the end of the intervention. Method of measurement: Visual Analogue Scale (VAS).;The severity of pain. Timepoint: 3 times within 20 minutes and 120 minutes after the end of the intervention. Method of measurement: Visual Analogue Scale (VAS). | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausea. Timepoint: 3 times within 20 minutes and 120 minutes after the end of the intervention. Method of measurement: Visual Analogue Scale (VAS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactTaghizadeh Mohsen
Kashan University of Medical Sciences
Outcome results
None listed