Uterocervical Angle and Preterm Labour

A

Ain Shams Maternity Hospital

Status

Unknown

Conditions

Preterm Labor

Treatments

Diagnostic Test: Uterocervical angle

Study type

Observational

Funder types

Other

Identifiers

NCT04532086
UCA in preterm birth

Details and patient eligibility

About

To determine whether a novel ultrasonographic marker, uterocervical angle, correlates with risk of spontaneous preterm birth

Full description

The uterocervical angle is the triangular segment measured between the lower uterine segment and the cervical canal, yielding a measurable angle. The first ray was placed from the internal os to the external os. The calipers were placed where the anterior and posterior walls of the cervix touch the internal and external os along the endocervical canal. If the cervix was curved, the first ray was also drawn from the internal os to the external os as a straight line. A second ray was then drawn to delineate the lower uterine segment. This ray was traced up the anterior uterine segment to a distance allowed by the preloaded image. Ideally, the second ray would reach 3cm up the lower uterine segment in order to establish an adequate measurement. The anterior angle in between the two rays was measured with a protractor. In the presence of funneling, the first ray was placed to measure the length of remaining cervix. The second caliper was placed from the innermost portion of measurable cervix and extended to the lower uterine segment. In the event that the lower uterine segment was found to be irregular, the second caliper was placed centrally along the segment. In the event of a retroverted uterus, the angle should be measured in a similar fashion with the first ray along the measurable cervix and the second ray traced along the lower uterine segment. Unlike in an anteverted or axial positioned uterus, however, the posterior side of the angle closer to the intrauterine contents should then be measured.

Enrollment

197 estimated patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Maternal age (18_40). BMI (20_34). singleton gestations between (18 - 28) weeks. Multiparity. History of previous preterm deliveries or mid-trimesteric abortions.

Exclusion criteria

Loss of follow up. Preterm premature rupture of membranes(PPROM). Placental abnormalities. Past history of cervical operations. Multifetal pregnancy. Polyhydramnios. Steroids intake . Medically or obstetric indicated pregnancy termination. Serious maternal or fetal problems. Cerclage during current pregnancy before the screening.

Trial contacts and locations

0

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Central trial contact

Mohammed Sh Abd Al Razik

Data sourced from clinicaltrials.gov

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