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Umbilical Cord clinical trials

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NCT ID: NCT01216865 Not yet recruiting - Diabetic Foot Clinical Trials

Umbilical Cord Mesenchymal Stem Cells Injection for Diabetic Foot

Start date: January 2011
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 diabetic foot is safe and effective in the management of diabetic foot ischemia, the therapeutic effect of stem cells is caused by improving blood circulation in ischemic limb which would in turn promote ulcer healing, prevent amputation of limb and relieve the Sevier pain of ischemia.

NCT ID: NCT01029496 Unknown status - Newborn Clinical Trials

Immediate VS Delayed Cord Clamping on Newborns

Start date: September 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The best time of the umbilical cord clamping has not been fully understood. immediate cord clamping (with in 10 seconds after birth) has been standardized practice for many years, while WHO protocol recommends to wait for 60-90 seconds. but the umbilical cord may still pulse for more than 90 seconds. is it best to wait longer until the pulsing ceased? how the time of umbilical cord will affect the newborn? will the longer time be less umbilical bleeding and shorter departure time of the cord? the hypothesis of this study is: to cut the cord after the pulsing ceased is the best time for cord clamping and will result in better quality of life for the newborn and less cord bleeding and earlier departure time of the cord, that means less infections of the cord.

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.