postpartum after pain. Postpartum care and examination
Conditions
Interventions
Intervention 1: control group:The samples were given a Mefenamic Acid oral capsule 250mg ,one hour after delivery then every 6 hours for 24 hours. Intervention 2: Intervention group: The samples we
Treatment - Drugs
control group:The samples were given a Mefenamic Acid oral capsule 250mg ,one hour after delivery then every 6 hours for 24 hours.
Intervention group: The samples were given a Anise oral capsule containing 60 mg of dried extracts of anise ( produced in Shahid Beheshti pharmacy faculty ), one hour after delivery then every 6 hour
Sponsors
vice chancellor for research of Shahid Beheshti University of Medical Sciences(SBUMS)
Eligibility
Sex/Gender
Female
Age
20 Years to 30 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Iranian; speak the Persian language; lives with his wife; they had normal vaginal delivery; single pregnancy with healthy baby; Gestational age between 37 to 42 weeks; the mother have the ability to breast-feeding; The baby can be feeding; mother for research is satisfied; women who suffer from postpartum pain; severity of postpartum pain is moderate to severe (scored more than 4 degree based on Numerical scale and need to use narcotics); normal vaginal delivery without devices (Vacuum, forceps); the mother does not have cesarean section and abdominal surgery history; Not used of epidural or spinal anesthesia; Non-smoking and drug abuse; the mother does not have a chronic disease (Hypertension, diabetes, heart disease, infectious diseases); No have allergy to Anise and other herbal drug; Exclusion criteria: herbal medicines or chemicals are used for pain relief during the study; the mother is suffering from serious complications after delivery (postpartum bleeding, temperature over 39 ° C, blood pressure higher than 140/90); continuation of breastfeeding to mother or baby is not possible causes; mother, for whatever reason are not willing to continue to participate in the study; foods containing spices are used during study
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity of pain. Timepoint: Before intervention, one hour after delivery then every 6 hours for 24 hours. Method of measurement: Numerical Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| The number of additional analgesic. Timepoint: one hour after delivery then every 6 hours for 24 hours. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactGity Ozgoli
Shahid Beheshti University of Medical Sciences
Outcome results
None listed