Skip to content

Digital Cervical and Cesarean Section

The Role of Digital Cervical Opening in Elective Cesarean Section

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03392077
Enrollment
300
Registered
2018-01-05
Start date
2018-01-01
Completion date
2019-02-01
Last updated
2019-09-24

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

Conditions

Caesarean Section

Brief summary

Cesarean delivery is one of the most commonly performed surgical operations worldwide Cesarean delivery even as an elective procedure has been associated with considerable maternal risks compared with vaginal delivery. Some of the complications include postpartum hemorrhage, uterine infection, urinary tract infection, wound infection, septicemia and maternal death. Over the years, many variations in the surgical technique of Cesarean delivery have been employed with the main purpose of improving its safety. A woman's cervix is firm and undilated at the beginning of pregnancy, but progressive remodeling occurs during gestation until the cervix is soft at term, especially the nulliparous cervix . The progressive dilatation of the cervix needs uterine contraction during labor. A mechanical dilatation of the cervix at cesarean section is defined as an artificial dilatation of the cervix performed by finger, sponge forceps or other instruments at non-labor cesarean section. According to a cochrane view The information currently available about the advantages of cervical dilatation at cesarean section is inconclusive. This may be due to small sample sizes and low power of statistic.

Interventions

PROCEDURECaesarean section

Caesarean section will be done to deliver the baby

Cervical dilatation will be done by double gloves digital dilatation postpartum

OTHERNo cervical dilatation

after delivery of the baby cervix will be remain closed

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years

Inclusion criteria

1. All women scheduled for elective cesarean section will be approached. 2. Women accepted to participate in the study participation after discussing the nature of the study.

Exclusion criteria

1. Immuno-compromised women. 2. Women suffering from any coagulation disorder or Blood disease. 3. Blood transfusion during surgery or before it. 4. History of wound infection or endometritis . 5. Ante partum hemorrhage. 6. History of long corticosteroid use. 7. Women refuse to participate in the study. 8. Suspected clinical evidence of infection. 9. anemic women 10. Multiple pregnancy 11. Preterm births 12. Rupture of membranes or chorioamnionitis 13. Women who use antibiotics during the last 24 hours due to any infection but not prophylactic antibiotic during caesarian section 14. Emergency caesarean section

Design outcomes

Primary

MeasureTime frame
The amount of postpartum blood loss (ml)24 hours

Countries

Egypt

Outcome results

None listed

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