The effect of Isosorbide Mononitrate on induction success

Phase 2

• Conditions: Other assisted single delivery.; Other assisted single delivery

• Registration Number: IRCT138803311946N3
• Lead Sponsor: Vice Chancellor for research, Guilan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 72

Inclusion Criteria

The inclusion criteria: 1-single pregnancy, 2- cephalic presentation, 3- Bishop Score =6, 4-normal AFI>5, 5- regular FHR, 6- intact membrane, 7- gestational age =37 weeks. Exclusion criteria are: Uterine contraction (=3 contraction 45’’ in 10 minutes) previous mymomectomy, history of headache, intolerance IMN, cardiopulmonary disease, vaso previa or placenta previa, cord prolepses, classic incision or previous myomectomy, irregular FHR, multiple pregnancy, macrosomia, polyhydramious, severe preeclampsia, maternal short stature.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
abor course. Timepoint: Hospitalization to delivery. Method of measurement: Based on Documented data.;Delivery mode. Timepoint: Post partum. Method of measurement: Based on Documented data.;Bleeding volume in labor and post partum. Timepoint: Control of labor course. Method of measurement: Based on Documented data.;Hospitalization duration and active phase initiation. Timepoint: Control of labor course. Method of measurement: Based on Documented data.

Secondary Outcome Measures

Name	Time	Method
ewborn apgar score. Timepoint: Immediately after delivery. Method of measurement: Based on documented data.;NICU requirement. Timepoint: Post partum. Method of measurement: Based on documented data.;The rate of maternal palpitation. Timepoint: During labor. Method of measurement: Based on documented data.;The occurance of maternal headache. Timepoint: Control during labor & delivery. Method of measurement: Based on documented data.;The ocurrance of tachysystol/hypersystol and hyperstimulated syndrome. Timepoint: FHR monitoring during labor. Method of measurement: Based on documented data.