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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.


Clinical Trial 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 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04274062
Study type Observational
Source Woman's Health University Hospital, Egypt
Contact
Status Completed
Phase
Start date May 1, 2019
Completion date December 2, 2020

See also
  Status Clinical Trial Phase
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