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Hemorrhage clinical trials

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NCT ID: NCT05080881 Withdrawn - Blood Loss Clinical Trials

Noninvasive Monitor of Vascular Volume Fluid Shifts

Start date: December 15, 2021
Phase: N/A
Study type: Interventional

Blood volume measurements are a critical step in the emergency care of trauma patients. The typical approach to this is to rely on historical information, physical examination and metrics such as heart rate. There is currently no good real-time measure to track blood volume. This study investigates the use of phonocardiography (listening to the sounds made by the heart) to track changes in central blood volume.

NCT ID: NCT05079815 Not yet recruiting - Clinical trials for Heavy Menstrual Bleeding

Heavy Menstrual Bleeding and Iron Deficiency Anemia

Start date: May 1, 2024
Phase:
Study type: Observational

In the present study, we test the ability of AMSS as a simple tool to identify women with HMB who have ID/ IDA. We will compare the AMSS score to patients' hemoglobin and serum ferritin in women with self-reported HMB and women with normal menstrual flow.

NCT ID: NCT05079061 Not yet recruiting - Clinical trials for Delivery Complication

A Trial of Sublingual Misoprostol to Reduce Primary Postpartum Haemorrhage After Vaginal Delivery

Start date: April 2022
Phase: Phase 4
Study type: Interventional

The objective of the randomized controlled study is to compare combination of sublingual misoprostol and routine uterotonics versus routine uterotonics alone on PPH in low risk women after vaginal delivery. The hypothesis is that combination of sublingual misoprostol and routine uterotonics is more effective than routine uterotonics alone in reduction of PPH in low risk women after vaginal delivery.

NCT ID: NCT05077540 Not yet recruiting - Labor Complication Clinical Trials

Oxytocin Versus, Sublingual Misoprostol in the Secondary Prevention of Postpartum Hemorrhage After Vaginal Delivery

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

Researchers sought to see how oxytocin versus, sublingual misoprostol affected estimated and measured blood loss during vaginal delivery in women who had blood loss >300 ml .

NCT ID: NCT05077124 Recruiting - Clinical trials for Blood Loss, Surgical

Safe and Timely Antithrombotic Removal (STAR) Registry

Start date: September 30, 2021
Phase:
Study type: Observational

This registry will capture real-world clinical use patterns and associated clinical outcomes with the use of CytoSorb for the removal of antithrombotic agents.

NCT ID: NCT05075486 Withdrawn - Mortality Clinical Trials

Quality Improvement to Reduce Mortality or Severe Intracranial Hemorrhage in Neonatal Extracorporeal Life Support

Start date: January 1, 2024
Phase: N/A
Study type: Interventional

This is a three-year pre- and post- interventional study to assess the effectiveness of collaborative quality improvement interventions on reducing mortality and severe intracranial hemorrhage (ICH) for neonates receiving extracorporeal life support (ECLS) in China.

NCT ID: NCT05075369 Not yet recruiting - Clinical trials for Normal Tension Glaucoma

Water Drinking Test Study and Disc Hemorrhages in Normal Tension Glaucoma

Start date: October 2021
Phase: N/A
Study type: Interventional

Disc hemorrhages are a known risk factor for progression of glaucoma. A positive water drinking test is also associated with progression of primary open glaucoma. The purpose of this study is to determine if patients with normal tension glaucoma and disc hemorrhages have a positive water drinking test. Patients with normal tension glaucoma and a disc hemorrhage will be recruited to undergo a water drinking test prior to any change in their treatment.

NCT ID: NCT05072873 Not yet recruiting - Clinical trials for Cesarean Section Complications

Topical Tranexamic Acid for the Prevention of Postpartum Hemorrhage in Women With Twin Pregnancy

Start date: October 1, 2021
Phase: N/A
Study type: Interventional

twin pregnant women requesting cesarean section, the effectiveness and safety of temporary uterine packing coupled with topical tranexamic acid as an adjuvant for decreasing blood loss during delivery were compared to placebo.

NCT ID: NCT05072860 Not yet recruiting - Clinical trials for Cesarean Section Complications

Topical Tranexamic Acid for the Prevention of Postpartum Hemorrhage in Women Undergoing Elective Cesarean Section

Start date: October 1, 2021
Phase: N/A
Study type: Interventional

In hypertensive women having an elective cesarean section, the effectiveness and safety of temporary uterine packing coupled with topical tranexamic acid as an adjuvant for decreasing blood loss during delivery were compared to placebo.

NCT ID: NCT05072769 Not yet recruiting - Uterus Involution Clinical Trials

Date Consumption and Uterine Involution

Start date: October 1, 2021
Phase: N/A
Study type: Interventional

There are many studies in the literature examining the effects of dates on pregnancy, birth and postpartum processes. However, no study has been found that examines the effect of women on the involution process in the early postpartum period. It is thought that this study will fill the gap in the literature with this study, which was conducted to determine the effect of date fed to women in the early postpartum period on uterine involution. The study was planned as a randomized controlled and experimental study to determine the effect of date fed to women in the early postpartum period on uterine involution. It will be held in the postpartum service of Sakarya University Training and Research Hospital between October - April 2021.