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Obstetric Complication clinical trials

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NCT ID: NCT03757598 Completed - Newborn Morbidity Clinical Trials

ePartogram Effectiveness Study in Kenya

Start date: August 1, 2016
Phase: N/A
Study type: Interventional

Quasi-experimental study to evaluate whether clinical care offered to clients was more appropriate and in line with WHO recommendations for care in normally progressing labor and in labor with complications, among providers using the novel intervention, ePartogram (an electronic version of the WHO paper partograph) vs. providers who offered care using the standard paper partograph, and whether fetal/newborn outcomes were improved among cases where partograph was used.

NCT ID: NCT03653884 Completed - Clinical trials for Obstetric Complication

Intra-abdominal Umbilical Vein Aneurysm

AVO
Start date: January 22, 2018
Phase:
Study type: Observational

The purpose of this study is to investigate the ultrasound characteristics and outcome of pregnancies with fetal Intra-abdominal umbilical vein aneurysm.

NCT ID: NCT03522909 Completed - Communication Clinical Trials

The Center for Peripartum Optimization

Start date: January 2017
Phase:
Study type: Observational

In January 2017 investigators started a Center for Peripartum Optimization (CPO) with the aim of optimizing a patient's clinical status in an outpatient setting to minimize unnecessary laboratory tests and studies, costly inpatient consultations, the likelihood of post-surgical adverse events, escalations in level of care, inpatient admissions and readmissions. This research project seeks to evaluate the impact of this innovative concept on patient outcomes during the last 12 months. Investigators will accomplish this by collecting retrospective data from patients' electronic medical records in the intervention group and comparing it to data gathered from a controlled group of patients with similar comorbidities but who were not evaluated at the CPO clinic.

NCT ID: NCT03478163 Terminated - Clinical trials for Postpartum Hemorrhage

Antibiotics During Intrauterine Balloon Tamponade Placement

Start date: March 8, 2018
Phase: Phase 4
Study type: Interventional

The goal of this study is to identify whether antibiotics given at the time of placement of an intrauterine balloon tamponade (IBT) will result in reduction of the risk of endometritis. The investigators hypothesize that antibiotics given at the time of intrauterine balloon tamponade will reduce the likelihood of postpartum endometritis.

NCT ID: NCT03161184 Completed - Clinical trials for Obstetric Complication

Impact of a Smartphone Intervention on Tanzanian Women's Childbirth Location

SUSTAIN1
Start date: July 23, 2013
Phase: N/A
Study type: Interventional

This study investigates whether training Community Health Workers (CHW) to use a smartphone-based prenatal counseling application as a "job aid" instead of the existing paper based standard is associated with increased women's use of maternal health services in Singida region, Tanzania.