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Effects of Peri Partum Integrated Nursing Care Versus Routine Care in Placenta Previa : A Randomized Controlled Trail

NCT ID: NCT04274062

Last Updated: 2020-12-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-05-01

Study Completion Date

2020-12-02

Brief Summary

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At our institution, the annual number of placenta previa was 494 cases (1.7%); of whom 95 cases (19.2%) were proved to have a placenta accreta. Perioperatively, they are subjected to regular care of a tertiary university hospital. This study aims to determine the effectiveness of peri partum integrated nursing care for the patients with placenta previa versus routine care.

Detailed Description

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Study design:

Experimental design: (randomized control trail)

Setting:

This study will be conducted at Woman's Health Hospital, Assiut University, emergency department and inpatient department.

Sample:

A convenience sample will be used, the total sample will include (100) patients with placenta previa, divided into two group1:1

* group 1: 50 patients study group
* group2: 50 patients control group

Conditions

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Placenta Previa Total Nursing Role

Keywords

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placenta previa Nursing antepartum hemorrhage randomized trial

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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peri partum integrated nursing care of placenta previa

* Part (1) personal data:
* Part (2) baseline and characteristics of the patients participants:
* Tool II- An observation checklist: This tool is develop by researcher according to guideline of Royal College of Obstetricians and Gynaecologists, 2018), and divide into three main parts: preoperative, intraoperative and postoperative.
* Part (1) pre-operative: includes assessment of :
* patients general condition
* investigation
* reserved blood
* Hemoglobin level
* Impact of hysterectomy option. -9-

Part (2) Intra-operative:

Includes assessment of :-

* Investigation
* Vital signs
* Hypothermia
* Blood loss
* I.V fluid
* Blood gases
* Fetal condition and APGAR score.
* Part (3) Post-operative: Includes:
* maternal complication
* fetal complication
* psychological satisfaction

Integrated Nursing care of placenta previa

Intervention Type PROCEDURE

Phase I :( preparation phase) Phase II: (Implementation phase) includes Preoperative care , intraoperative care and postoperative care by a nurse.

Phase III: (Evaluation phase)

peri partum regular care of placenta previa

Routine nursing care of all cases of placenta previa (preoperative, intraoperative and postoperative)..

Integrated Nursing care of placenta previa

Intervention Type PROCEDURE

Phase I :( preparation phase) Phase II: (Implementation phase) includes Preoperative care , intraoperative care and postoperative care by a nurse.

Phase III: (Evaluation phase)

Interventions

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Integrated Nursing care of placenta previa

Phase I :( preparation phase) Phase II: (Implementation phase) includes Preoperative care , intraoperative care and postoperative care by a nurse.

Phase III: (Evaluation phase)

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Pregnant women with diagnosis of placenta previa.

Exclusion Criteria

* Other high risk pregnancy cases
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Woman's Health University Hospital, Egypt

OTHER

Sponsor Role lead

Responsible Party

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Professor Atef Darwish

Professor of Obstetrics and Gynecology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Atef Darwish

Role: PRINCIPAL_INVESTIGATOR

Woman's Health University Hospital

Locations

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Woman's Health University Hospital

Asyut, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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Randomized controlled trial

Identifier Type: -

Identifier Source: org_study_id