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Does mechanical dilatation of the cervix at non-labour caesarean section reduce postoperative morbidity?

Completed
Conditions
Efficacy of mechanical dilatation of the cervix at non-labour caesarean section
Reproductive Health and Childbirth - Childbirth and postnatal care
Registration Number
ACTRN12612000228886
Lead Sponsor
Sven Kehl
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
500
Inclusion Criteria

Greater than 23+6 weeks of gestation, non-labour caesarean section

Exclusion Criteria

Sign of infection, running antibiotic therapy, opening of the cervix

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postpartum Hemorrhage (blood loss more than 1000 ml) - assessed by clinical assessment[24 hours after childbirth]
Secondary Outcome Measures
NameTimeMethod
Blood transfusion needed - e.g. hemoblobin level below 7 g/dl[Within 6 weeks after childbirth.];Hemoglobin - indicates blood loss (assessed by blood analysis)[Day 1 after childbirth];Secondary postpartum hemorrhage - assessed by clinical assessment[Within 6 weeks after childbirth.];Infection - assessed by clinical assessment (temperatur greater than 38,5 degrees C, blood tests - e.g. CRP)[Within 6 weeks after childbirth.];Cervical trauma - assessed by clinical assessment[After childbirth];Subinvolution - assessed by clinical assessment[Day 5 after childbirth.];Time of surgery - assessed by medical records data[After surgery.]
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