The Effect of IV PAPAVERINE 80 mg Prior to Catheter Balloon Insertion on Bishop Score and Pain
Induction of Labor, Pain, Acute, Labor Pain
About this trial
This is an interventional treatment trial for Induction of Labor focused on measuring Induction of labor, Ripenning of the cervix, Catheter balloon, Antispasmodic
Eligibility Criteria
Inclusion Criteria: Women with a singleton pregnancy, over the age of 18, pregnant at term (ie between weeks 37-42) Bishop score is less than 6, for which a medical decision was made regarding the induction of labor by catheter Vertex presentation, intact membranes Viable fetus Exclusion Criteria: Twin pregnancy Women after caesarean section Severe fetal anomalies Women with vaginismus or vulvodynia Women with psychiatric illnesses including depression and schizophrenia Contraindication for vaginal delivery A woman who is unable to sign a consent form Women are known for supraventricular tachycardia Women with tachycardia over 100 or arrhythmia Known sensitivity to one of the components of the drug Liver disease
Sites / Locations
- Galilee Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
Intervention group- IV PAPAVERINE 80 mg
Conrol group- Placebo group.
Administration of IV PAPAVERINE 80 mg in 100 ml of saline, once within half an hour before inserting a single-balloon balloon catheter
Administration of 100 ml of saline within half an hour before the insertion of a single-balloon catheter