Modified Cervical Inversion During CS in Placenta Previa

Alalfy Modofied Cervical Inversion During CS in Placenta Previa

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03772184

Enrollment

240

Registered

2018-12-11

Start date

2019-01-10

Completion date

2019-05-15

Last updated

2022-02-22

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

Conditions

Placenta Previa

Brief summary

There is an increasing rates of placenta previa nowadays

Detailed description

several techniques were described to control bleeding .

Interventions

PROCEDURECervical inversion

inverting the cervical lip after delivery

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

PREVENTION

Masking

QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

Using cervical inversion during cesarean section

Eligibility

Sex/Gender

FEMALE

Age

22 Years to 40 Years

Healthy volunteers

Yes

Inclusion criteria

* pregnant women 38 weeks or more with placenta previa

Exclusion criteria

* pregnant ladies with normally implanted placenta or placenta accreat , increta or percreta

Design outcomes

Primary

Measure	Time frame	Description
The number of women whose placental bed bleeding will be controlled by cervical inversion cervical inversion	within an hour	how can the cervical inversion technique controls the placental bed bleeding

Countries

Egypt

Outcome results

None listed

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