Status:
UNKNOWN
Cervical Length in Cases of Placenta Previa
Lead Sponsor:
Cairo University
Conditions:
Placenta Previa
Eligibility:
FEMALE
25-40 years
Brief Summary
This study establishes the relationship between cervical length and whether it can be used to predict haemorrhage and preterm delivery in cases of placenta previa.
Detailed Description
Some studies have reported an association between ultrasonographic decreased cervical length and the likelihood of complications as antepartum or post-partum haemorrhage requiring an emergency caesare...
Eligibility Criteria
Inclusion
- Age: 20-45 years old
- Single Pregnancy
- Fetal gestational age 28 to \< 36 weeks
- Normal amniotic fluid index (AFI)
- Diagnosis of placenta previa by pelvic ultrasound that was confirmed when the lower placental edge overlies the internal cervical os on transvaginal ultrasound (TVS).
Exclusion
- Threatened preterm labor and maternal use of vaginal progesterone.
- Preterm premature rupture of membranes;
- Polyhydramnios;
- Presence of cercelage and history of cervical cone biopsy which both affect cervical length.
- Diagnosis of multiple fetal anomalies;
- Women with other risk factors for intra-partum hemorrhage
Key Trial Info
Start Date :
March 1 2018
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
July 15 2018
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT03451136
Start Date
March 1 2018
End Date
July 15 2018
Last Update
March 1 2018
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