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Assessment of Maternal and Perinatal Morbidity and Mortality in Vaginal and Cesarean Delivery

Assessment of Maternal and Perinatal Morbidity and Mortality in Vaginal and Cesarean Delivery Among a Sample of Women Delivering at Ain Shams University Maternity Hospital

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03666078
Enrollment
100
Registered
2018-09-11
Start date
2018-07-15
Completion date
2019-04-01
Last updated
2019-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delivery,Complication,Fetal, Delivery ,Complications,Maternal

Brief summary

This study will be done at Ain Shams university maternity hospital to identify the significant risk of maternal intensive care unit admission, need for advanced surgery, postpartum hemorrhage, need for blood transfusion, febrile morbidity, neonatal intensive care unit admission (NICU), need for neonatal intubation and low APGAR scoring in both vaginal and cesarean section .and this will lead us to know if cesarean section rates in our unit is a safe alternative to vaginal delivery and which of both maneuvers will introduce fewer hazards to mother and fetus.

Detailed description

* Type of Study: a cross-sectional study * Study Setting: Ain Shams maternity hospital * Study Period: 6 months * Study Population: in this prospective study, all women who deliver vaginally and by cesarean section at Ain Shams maternity hospital will be included. * Sampling Method: All of the pregnant women who will deliver vaginally and all of pregnant women who will deliver by cesarean sections in the labor delivery room at Ain Shams University Maternity Hospital on a fixed day and by a fixed team over a period of 6 months * Sample Size: all pregnant women who will deliver at Ain Shams maternity hospital. * Inclusion criteria : * All of the patients who will deliver vaginally * All of the patients who will deliver by cesarean sections. * Exclusion criteria: no exclusion criteria, all women who will attend for delivery will be included. * Ethical Considerations: the study objectives will be briefly and clearly described to all participants and an oral consent will be obtained from all patients. * Study Procedures : In all selected cases the following will be recorded: Parameters of maternal morbidity: 1. ICU admission due to the complication of delivery. 2. Need for advanced surgery (int. iliac ligation -hysterectomy -or due to the injury of pelvic organs). 3. Febrile morbidity temp >38C on two or more occasion within 48h of delivery. 4. Postpartum hemorrhage (blood loss 500cc in VD and 1liter in C\\S). 5. Wound infection. 6. Late complications e.g. (D.V.T-puerperal sepsis and hematoma). 7. Need for blood transfusion post labor 8. Maternal mortality. Parameters of fetal morbidity: 1. Intracranial hemorrhage as compilations of delivery. 2. Neonatal ICU admission as compilations of delivery 3. Fracture (Femur, ribs, and humorous) 4. Meconium aspiration. 5. Erb's palsy. 6. APGARscore1-5. 7. Need for intubation during resuscitation. * Statistical analysis The patient will be subdivided into 4 groups, normal VD, instrumental VD, emergency C\\S, and elective C\\S The data has been collected in analytical sheet tabulated and statistical analysis using the following tests 1- T-test. 2- Chi-square test. 3- Fisher exact test Statistical package : data analysis will be performed by SPSS 16.0 using descriptive statistics tools, including mean, standard deviation and figures.A t-test will be used to compare mean values of the two groups .P-values, smaller than 0.05, were considered statistically significant.

Interventions

PROCEDUREcesarean delivery

women delivered by cesarean section

Sponsors

Alzahraa Ismail Ragheb Goda
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 48 Years
Healthy volunteers
No

Inclusion criteria

* All of the patients who will deliver vaginally * All of the patients who will deliver by cesarean sections.

Exclusion criteria

* no

Design outcomes

Primary

MeasureTime frameDescription
labor and delivery outcome24 hoursdocument maternal and perinatal morbidity

Countries

Egypt

Contacts

Primary ContactMohamed M Samy, MD
Mohammedsamy8132@gmail.com01001947488
Backup ContactAhmed N Shaker
dr_nagy.ahmed@yahoo.com01098670624

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026