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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03113227
Other study ID # 5355
Secondary ID
Status Completed
Phase N/A
First received April 10, 2017
Last updated July 13, 2017
Start date April 15, 2017
Est. completion date July 9, 2017

Study information

Verified date July 2017
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Seventy ladies indicated for induction of delivery will be recruited. Two ways of assessment of their cervices will be done before actual induction of labor. First, ultrasound will be done to assess the angle and the length of the cervix. Then vaginal examination will be done to assess the characteristics of cervix. Analysis will be done to identify the best predictor of successful induction of labour.


Description:

Seventy patients indicated for induction of labor will be recruited. Two ways of assessment of their cervices will be done before actual induction of labor. First, transvaginal ultrasound will be done to assess the posterior angle and the length of the cervix. Then vaginal examination will be done to measure the Bishop score. Analysis will be done to identify the best predictor of successful induction of labour.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date July 9, 2017
Est. primary completion date July 9, 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 37 Years
Eligibility Inclusion Criteria:

- Singleton pregnancy

- Gestational age between 35 and 42

- Presence of an indication for induction of labour as post-term pregnancy or rupture of membranes

- The fetus is living

- Cephalic presentation

Exclusion Criteria:

- Estimated fetal weight more than 4 kilograms

- Malpresentation

- Oligohydramnios

- Polyhydramnios

- Non-reassuring non-stress test before induction of labor

- Cephalo-pelvic disproportion

- Previous operation on the cervix as cautery or cerclage

- Previous cesarean section

- Any contraindication to vaginal delivery including placenta previa

- Anomalous fetus

- Morbid obesity

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Transvaginal ultrasound
Transvaginal ultrasound will be made for assessment of posterior cervical angle and cervical length
Vaginal examination
Vaginal examination will be done for assessment of Bishop score

Locations

Country Name City State
Egypt Department of Obstetrics and Gynecology, Kasr Al-Ainy hospital Cairo Greater Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Value of posterior cervical angle Value of posterior cervical angle will be measured by an investigator At around 10 minutes from admission to hospital
Secondary Length of the cervix Length of the cervix will be measured by an investigator At around 10 minutes from admission to hospital
Secondary Bishop score Bishop score will be measured by an investigator At around 30 minutes from admission to hospital
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