Evaluation of the effect of oral hyoscine on the rate of cervical opening in term pregnancy

Phase 3

Recruiting

Conditions: Pregnancy.

Registration Number: IRCT20180819040830N1

Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 100

Inclusion Criteria

Age older than 18 years
Primiparous
Gestational age of 39 weeks and 0 days to 40 weeks and 0 days
Spontaneous pregnancy
Singleton pregnancy
Cephalic presentation
Bishop score equal to or less than 5

Exclusion Criteria

The existence of a placenta previa or placenta detachment (decollement)
Fetal distress
The presence of IUGR or macrosomal infant (embryo weighing more than 4000 gr)
The presence of underlying illness, such as diabetes or pre-pregnancy or pre-pregnancy hypertension
History of cervix trauma
Hyoscine susceptibility
History of cervical or uterine surgery
Using narcotic drugs or analgesics
The presence of glaucoma
The presence of cardiovascular disease or tachycardia more than 100 beats per minute

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Cervix status. Timepoint: At the time of entering the design, 24 hours later, and then every 72 hours until delivery and at the time of delivery. Method of measurement: The Bishop Score gives points to 5 measurements of the pelvic examination dilation, effacement of the cervix, station of the fetus, consistency of the cervix, and position of the cervix and its rage is 0 to 13.

Secondary Outcome Measures

Name	Time	Method
Gestational age at delivery time. Timepoint: At delivery time. Method of measurement: Ask the patient.;Delivery type. Timepoint: At delivery. Method of measurement: Normal vaginal delivery (NVD), Cesarean section (C/S).