Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-24 @ 4:37 PM
Ignite Modification Date:
2025-12-24 @ 4:37 PM
NCT ID:
NCT03098966
Brief Summary:
The purpose of the study to evaluate the practice and short term maternal and perinatal outcomes of trial of labor after cesarean section offered to women at Ain Shams University Maternity Hospital (ASUMH) during the 3-year period from January 2013 to December 2015.
Detailed Description:
This is a retrospective study that was performed at Ain Shams University Maternity Hospital.
The following data will be gathered (whenever available), tabulated and subjected to the proper statistical analysis:
History:
* Age
* Duration of marriage
* Inter-pregnancy interval
* Gestational age (by menstrual dates or US)
* Obstetric history (parity, mode of delivery, assisted vaginal delivery, previous vaginal birth after cesarean section, neonatal outcome)
* Present and past history of any medical, surgical or obstetric problems; history of infection after previous CS
General examination:
* General condition
* Vital data
Abdominal examination:
* Fundal level
* Estimated fetal weight (clinically or by US)
* Scar tenderness
Vaginal examination on admission:
* Cervical status
* Station of presenting part
* Membranes status
* Pelvic adequacy
Investigations performed:
* Complete Blood Count
* Ultrasonography
Intrapartum management:
* Progress and duration of labor according to partogram (or admission-delivery time)
* Intrapartum complications; placental abruption, uterine rupture, hysterectomy, complications during surgical intervention if any
Mode of delivery:
* Vaginal delivery (spontaneous, assisted, complications)
* Cesarean section (indication, scar dehiscence)
Postpartum Data:
* Postpartum hemorrhage
* Blood transfusion
* Neonatal outcome; fetal weight, birth trauma, Neonatal Intensive Care Unit admission, mortality
Study:
NCT03098966
Study Brief:
Protocol Section:
NCT03098966