ClinicalTrials.Veeva

Menu

The Cervical Length and Thickness of Cesarean Section Scar With Preterm Labor

A

Assiut University

Status

Completed

Conditions

Preterm Labor

Treatments

Radiation: Ultrasound

Study type

Interventional

Funder types

Other

Identifiers

NCT04554745
Preterm labor and previous cs

Details and patient eligibility

About

Although the Cesarean section is one of the most common obstetric operations around the world, the World Health Organization recognizes that where cesarean rates are higher than 10%, there is no increase in beneficial maternal and newborn outcomes. some researchers noted that in countries where cesarean rates are above 15%, populations experience higher maternal, infant, and neonatal mortality rates. infants born by cesarean delivery are more likely to require neonatal intensive care unit and have greater respiratory complications, and higher odds for childhood asthma, and obesity.

Preterm is defined as babies born alive before completing 37 weeks of pregnancy.

Preventing Preterm birth is a global priority due to increased risk for neonatal morbidity and mortality.

Enrollment

260 patients

Sex

Female

Ages

20 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. singleton pregnant
  2. gestational age at 18 weeks
  3. previous vaginal or Cesarean section

Exclusion criteria

  1. twins pregnancy in their second birth
  2. previous preterm labor
  3. diabetic during the second pregnancy
  4. hypertensive during the second pregnancy
  5. cigarette use during the second pregnancy
  6. congenital anomalies

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

260 participants in 2 patient groups

Non-scared uterus of pregnant women
Other group
Treatment:
Radiation: Ultrasound
Scared uterus of pregnant women
Other group
Treatment:
Radiation: Ultrasound

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems