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Trial record 29 of 12496 for:    cervical

Cervical Intervention During Cesarean Section

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT03772184
Recruitment Status : Completed
First Posted : December 11, 2018
Last Update Posted : June 10, 2019
Sponsor:
Collaborator:
Suez Canal University
Information provided by (Responsible Party):
Mahmoud Alalfy, Aljazeera Hospital

Brief Summary:
There is an increasing rates of placenta previa nowadays

Condition or disease Intervention/treatment Phase
Placenta Previa Procedure: Cervical inversion Not Applicable

Detailed Description:
several techniques were described to control bleeding .

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 240 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Using cervical inversion during cesarean section
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Cervical Intervention During Cesarean Section in Placenta Previa
Actual Study Start Date : January 10, 2019
Actual Primary Completion Date : May 12, 2019
Actual Study Completion Date : May 15, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Cesarean Section

Arm Intervention/treatment
Active Comparator: cervical inversion Procedure: Cervical inversion
inverting the cervical lip after delivery

No Intervention: no cervical inversion



Primary Outcome Measures :
  1. The number of women whose placental bed bleeding will be controlled by cervical inversion cervical inversion [ Time Frame: within an hour ]
    how can the cervical inversion technique controls the placental bed bleeding



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Ages Eligible for Study:   20 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Gender Based Eligibility:   Yes
Gender Eligibility Description:   pregnant women with placenta previa
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • pregnant women 38 weeks with placenta previa or focal accreta

Exclusion Criteria:

  • pregnant ladies with normally implanted placenta

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03772184


Locations
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Egypt
Algazeerah and Kasralainy hospital
Giza, Egypt
Sponsors and Collaborators
Aljazeera Hospital
Suez Canal University
Investigators
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Principal Investigator: Mahmoud Alalfy, PhD National research centre , Aljazeerah hospital

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Responsible Party: Mahmoud Alalfy, Lecturer Obstetrics and Gyneology , National Research Centre, Aljazeera Hospital
ClinicalTrials.gov Identifier: NCT03772184     History of Changes
Other Study ID Numbers: cervical manipulation
First Posted: December 11, 2018    Key Record Dates
Last Update Posted: June 10, 2019
Last Verified: June 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
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Placenta Previa
Obstetric Labor Complications
Pregnancy Complications
Placenta Diseases