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Umbilical Cord clinical trials

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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: NCT02760966 Recruiting - Umbilical Cord Clinical Trials

Effectiveness of Alcohol 70º vs Soap on Cord Separation Time and the Complication in the Newborn

Start date: October 2015
Phase: N/A
Study type: Interventional

Evaluate the effectiveness of alcohol 70º compared with soap on cord separation time and the complication rate in the newborn.

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: NCT01224327 Not yet recruiting - Liver Cirrhosis Clinical Trials

Umbilical Cord Mesenchymal Stem Cells Infusion Via Hepatic Artery in Cirrhosis Patients

Start date: October 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to investigate the efficacy of umbilical cord mesenchymal stem cells (MSCs) infusion via hepatic artery in the treatment of liver cirrhosis.

NCT ID: NCT01221428 Active, not recruiting - Ulcerative Colitis Clinical Trials

Umbilical Cord Mesenchymal Stem Cells Infusion for Ulcerative Colitis

Start date: September 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether umbilical cord Mesenchymal Stem Cells of treatment for ulcerative colitis is safe and effective.

NCT ID: NCT01219465 Active, not recruiting - Diabetes Mellitus Clinical Trials

Umbilical Cord Mesenchymal Stem Cells Infusion for Initial Type 1 Diabetes Mellitus

Start date: September 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether umbilical cord Mesenchymal Stem Cells of treatment for initial type 1 diabetes is safe and effective.