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Randomized Comparison of Sharp Versus Blunt Techniques at Cesarean

Unintended Extension of the Lower Segment Uterine Incision at Cesarean Delivery;A Randomized Comparison of Sharp Versus Blunt Techniques

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01519440
Enrollment
1076
Registered
2012-01-27
Start date
2011-03-31
Completion date
2012-02-29
Last updated
2012-10-23

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

Conditions

Disruption of Uterine Incision After Cesarean Section

Keywords

unintended extension, blunt, sharp, maternal blood loss

Brief summary

The purpose of this study is to determine whether a specific surgical technique, blunt compared with sharp expansion of the transverse lower uterine incision, is associated with risk of unintended extension of uterine incision

Interventions

None listed

Sponsors

Istanbul Bakirkoy Maternity and Children Diseases Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

1. Term pregnancy(\> 38 weeks of gestation) 2. Required elective cesarean delivery 3. maternal age between 18-40 years

Exclusion criteria

1. Required emergency cesarean delivery 2. Abnormal presentation 3. Planned cesarean hysterectomy 4. History of low segment vertical uterine incision 5. History of classical upper segment uterine incision 6. multiple pregnancy 7. cases with a high risk for bleeding(HELLP send, preeclampsia, placental insertion anomalies) 8. Grand multiparity(parity\>5)

Design outcomes

Primary

MeasureTime frame
unintended extension of uterine incisionduring the operation

Secondary

MeasureTime frame
intraoperative maternal blood lossafter 48 hours than operation

Countries

Turkey (Türkiye)

Outcome results

None listed

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