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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04274062
Other study ID # Randomized controlled trial
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2019
Est. completion date December 2, 2020

Study information

Verified date December 2020
Source Woman's Health University Hospital, Egypt
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

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


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 2, 2020
Est. primary completion date November 1, 2020
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - Pregnant women with diagnosis of placenta previa. Exclusion Criteria: - Other high risk pregnancy cases

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
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)

Locations

Country Name City State
Egypt Woman's Health University Hospital Assiut

Sponsors (1)

Lead Sponsor Collaborator
Woman's Health University Hospital, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improved maternal and fetal well beings in cases of placenta previa Adding an integrated nursing care to the regular care of cases of placenta previa 2 years
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