The study was a clinical trial conducted from December 2013 to June 2014 in Ahvaz city, Khuzestan province, South-West of Iran. Among the pregnant women referring to Sina Hospital for weekly visits, 100 eligible pregnant women were selected after examination by an obstetrician, and then were randomly allocated to control and case groups using a random number table. The sample size was at least 50 subjects for each group. Inclusion criteria were primigravida, 41 - 42 weeks of gestation, starting prenatal care in the first trimester, body mass index (BMI) 19.8 - 26, cephalic presentation, singleton pregnancy, reactive non stress test (NST) and Bishop score 4 or less. Bishop score (also known as cervix score) is a pre-labor system to predict the need for labor induction. The five components to be assessed on vaginal examination includes: dilation, effacement and consistency of cervix, position and station of fetus. To assess the fetus, NST was taken for the eligible women; if it was reactive, a midwife explained the purpose of study for the participants and then they read and signed the written consent forms. Due to complications of post term pregnancies, according to some standard protocols, these pregnancies are terminated at this gestational age. Then, 0.018 g/kg of dill seeds and a teaspoon full of sugar was dissolved into 250 mL of boiling water and brewed for about 10 minutes. Subjects in the case group drank it once at the outset of entering. To determine the dose of the drug , the findings of an article assessing the effectiveness of oral dill seeds extracts on postpartum hemorrhage (
25) were used. The dill seeds were purchsed from Parsi Teb Company in Tehran. This solution was prepared at hospital by a midwife, and the control group was also given 250 mL of boiled water with a teaspoon full of sugar. The case group was infused with simple Ringer solution, but the control group received standard induction of labor with oxytocin (
2). The standard protocol was utilized for labor induction based on 10 units of oxytocin into 1000 mL of Ringer solution which started with four drops and added up four drops every 15 minutes to reach 64 drops. Regulation of solution droplets for the intervention group was similar to that of the controls. In both groups, fetal heart rate and contractions were checked every 15 minutes during the first stage of labor. Maternal vital signs were measured every four hours and if Rupture of membrane (ROM) occurred, temperature was measured once an hour. Vaginal examinations interval were done based on partograph, a chart established by WHO to manage the labor (
30). The inductions were performed by the first author a midwife under supervision of an obstetrician. ROM was performed at 3 - 4 cm of cervical dilation in both groups. In control group induction was infused for 8 hours. Both groups were given 24 hours to enter the labor phases. Both groups were controlled for the changes in Bishop score, latent and active phase duration, severity of labor pain in the first stage of labor, the second and third stage duration, also any maternal and fetal complications and when it happened, type of delivery, fetus gender, and Apgar score were recorded. Subjective pain was measured using a horizontal visual analog scale (VAS) in dilatation of 3 cm in latent and dilatation of 7 cm in active phase. Validity and reliability of this scale was confirmed in previous studies (
31). According to Friedman curve, cervical dilatation of 3 - 5 cm is the threshold of active phase of labor (
2) therefore, middle dilatation was selected in both groups to evaluate the severity of pain in latent and active phase. Duration of uterine contractions was evaluated by touching the uterus fundus. The vaginal examination was determined upon delivery characteristics of each subject. According to Friedman statement, latent phase begins by mother’s understanding of regular contractions associated with progressive dilatation of the cervix. Therefore, it was used to evaluate the latent phase. Moreover, Apgar score of neonates was recorded after delivery and in case of problems it was recorded carefully. Data were collected based on prenatal care form and then analyzed by SPSS software employing Chi-square test, T-test, Mann-Whitney and Fisher tests. P value was set as 0.05 for all analyses.
The study was approved by the Institutional Review Board and the local Research Ethics Committee in Ahvaz Jundishapur university of medical sciences as: Ajums.REC.1392, 159. The study also was recorded at IRCT system as: IRCT2014070518371N1.