Clinical Trials Logo

Umbilical Cord clinical trials

View clinical trials related to Umbilical Cord.

Filter by:
  • Completed  
  • Page 1

NCT ID: NCT05409885 Completed - Anesthesia, General Clinical Trials

The Effect of General and Spinal Anesthesia on Neutrophil-to-lymphocyte Ratio

Start date: March 20, 2022
Phase:
Study type: Observational

The aim of the study was to evaluate the effects of anesthetic techniques (general and spinal anesthesia) on umbilical cord neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR) and mean platelet volume (MPV) in patients undergoing cesarean section.

NCT ID: NCT03844490 Completed - Umbilical Cord Clinical Trials

Timing of Umbilical Cord Clamping: One to Three Minutes vs. After Cessation of Cord Pulsation

CORD
Start date: April 1, 2019
Phase: N/A
Study type: Interventional

The timing of umbilical cord clamping has been widely discussed in the scientific community. As part of the worldwide strategies to reduce childhood iron deficiency anemia, the incorporation of late clamping (at least one minute after delivery), has been adopted as an effective and low-cost measure for health services. The optimal timing for clamping, ( if until 3 minutes of delivery, or later, when the cord stops spontaneous pulse), still remains controversial. Also, doubts remain about the effect of late clamping of the umbilical cord on maternal outcomes. This study has the hypothesis that waiting for the cessation of the cord pulsation will not bring harm to the newborn or the mother.

NCT ID: NCT03694613 Completed - Preterm Infant Clinical Trials

Utility of Placental/Umbilical Cord Blood in Early Onset Neonatal Sepsis in Very Low Birth Weight Infants

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

This study evaluates the utility of placental/umbilical cord blood (PUCB) to perform the baseline workup testing for EONS in Very Low Birth Weight Infants: CBC (Complete Blood Count) with differential, Immature/Total ratio (I/T ratio), and blood culture along with CRP and IL-6 levels. A cohort (63 subjects) of preterm infants will be recruited. All the participants will be evaluated for sepsis using placental/umbilical cord blood (PUCB) and subject blood sample during the first 12 hours of life (after birth).

NCT ID: NCT02187510 Completed - Premature Infant Clinical Trials

Umbilical Cord Milking vs Delayed Cord Clamping in Preterm Infants Born by Cesarean Section

Start date: July 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the umbilical cord milking in preterm infants born by cesarian section less than 34 weeks is more effective than delayed cord clamping to obtain higher levels of hemoglobin.

NCT ID: NCT01367132 Completed - Umbilical Cord Clinical Trials

Assessment of the Number of Umbilical Cord Vessels at the Time of Nuchal Translucency Screening

Start date: February 2011
Phase: N/A
Study type: Observational

The primary objective of this study is to determine the detection rate of two- or three-vessel umbilical cord at the time of nuchal translucency screening between 11 and 13 6/7 weeks gestation. Hypothesis: Detection rate of the number of vessels during first trimester will be as accurate as the detection of vessels during the second trimester.

NCT ID: NCT01309321 Completed - Sepsis Clinical Trials

Perinatal Handwashing Intervention in Bangladesh

Start date: October 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if an intensive handwashing intervention administered to primiparous women during their pregnancy can increase maternal handwashing with soap at critical times.

NCT ID: NCT00345254 Completed - Umbilical Cord Clinical Trials

Severing Nuchal Cord at the Time of Delivery.

Start date: September 2003
Phase: Phase 1
Study type: Interventional

Umbilical cord often becomes encircled around portions of the fetus, usually the neck. The incidence ranges from 1 loop in 21% to 3 loops in 0.2%. In this study we wish to assessed the practice of severing the cord, which was encircled once around the neck of the fetus, after delivery of the anterior shoulder and prior to extraction of the body. The study and the control groups will include 30 women, each one. After diagnosis of cord around the neck during labor by ultrasound, the women will inter a randomization process. After delivery of the head, it will be cut intentionally in the study group and left intact in the control group. Neonatal outcome will be assessed.

NCT ID: NCT00127699 Completed - Infection Clinical Trials

Triple Dye Plus Alcohol Versus Triple Dye Alone for Newborn Umbilical Cord Care

Start date: August 2005
Phase: Phase 1
Study type: Interventional

In the United States (U.S.) there currently is no standard method of umbilical cord care, resulting in varying practices within and across institutions. These differences may result in an increase in morbidities for newborns such as the formation of umbilical granulomas and increases in acute care utilization. This study will determine which of two common methods of caring for newborn umbilical cords is superior - triple dye, followed by the application of rubbing alcohol, or triple dye alone.