ClinicalTrials.Veeva

Menu

Modified Cervical Inversion During CS in Placenta Previa

A

Aljazeera Hospital

Status

Completed

Conditions

Placenta Previa

Treatments

Procedure: Cervical inversion

Study type

Interventional

Funder types

Other

Identifiers

NCT03772184
Modified cervical inversion

Details and patient eligibility

About

There is an increasing rates of placenta previa nowadays

Full description

several techniques were described to control bleeding .

Enrollment

240 patients

Sex

Female

Ages

22 to 40 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

240 participants in 2 patient groups

cervical inversion
Active Comparator group
Treatment:
Procedure: Cervical inversion
no cervical inversion
No Intervention group

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems