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Hemorrhage clinical trials

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NCT ID: NCT02083809 Completed - Hemorrhage Clinical Trials

Effects of Oxytocin on Bleeding Outcomes During Dilation and Evacuation

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

Currently, there is very little research to identify ways to decrease blood loss during D&E (dilation and evacuation) procedures. The objective is to determine whether routine use of intravenous oxytocin will improve bleeding outcomes at the time of D&E at 18-24-weeks gestation. To evaluate the hypothesis, investigators will perform a randomized, double-blinded, placebo-controlled trial. The patient will be followed until discharged from the postoperative care unit during which time patient satisfaction, pain score and postoperative bleeding will be assessed.

NCT ID: NCT02083107 Completed - Clinical trials for Postpartum Hemorrhage

Comparison Between Rectal & Sublingual Misoprostol Before Caesarian Section To Reduce Intra & Post-Operative Blood Loss

Start date: February 2013
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of the work is to evaluate & compare the effectiveness of rectally administered PGE1 synthetic analogue (misoprostol) 400 microgram versus sublingually administered misoprostol before caesarean section to decrease blood loss during and after the operation.

NCT ID: NCT02081820 Completed - Hyperglycemia Clinical Trials

Admission HbA1C in Aneurysmal Subarachnoid Hemorrhage

Start date: July 2012
Phase: N/A
Study type: Observational [Patient Registry]

In patients suffering from aneurysmal subarachnoid hemorrhage (aSAH), hyperglycemia is considered an adverse prognostic factor. Glycated hemoglobin (or HbA1c) can be measured to estimate the average plasma glucose concentration over prolonged periods of time, thus determination of glycated hemoglobin at admission after aSAH serves as an approximation of blood glucose levels in the weeks preceding aneurysm rupture. In this patient registry admission HbA1c, clinical course and neurological outcome after 6 month are recorded, to determine whether elevated blood glucose levels prior to aneurysm rupture influence the clinical course and patient outcome after aSAH.

NCT ID: NCT02079558 Completed - Clinical trials for Postpartum Hemorrhage

Efficacy of Oxytocin vs. Carbetocin in Prevention of Postpartum Hemorrhage After Cesarean Section

Start date: September 2012
Phase: Phase 2
Study type: Interventional

Postpartum hemorrhage (PPH) is a common complication of childbirth and a leading cause of maternal morbidity and mortality. The prompt and effective treatment of subjects with PPH would reduce operation risks. Hence in this study, the efficacy of Oxytocin and Carbetocin was compared in prevention of postpartum hemorrhage after cesarean sections.

NCT ID: NCT02078037 Completed - Clinical trials for Intracerebral Hemorrhage

Systemic Normothermia in Intracerebral Hemorrhage (ICH)

SNICH
Start date: March 2014
Phase: Phase 0
Study type: Interventional

Patients with a supratentorial intracerebral hemorrhage will be randomly assigned to either the experimental group which will keep them at a normal body temperature or the standard of care group. The investigators propose to test the hypothesis that prophylactic forced normothermia in patients with ICH leads to less systemic inflammation and decreased perihematomal edema.

NCT ID: NCT02073890 Completed - Clinical trials for Traumatic Subarachnoid Haemorrhage

Neurological Outcome in Patients of Traumatic Subarachnoid Haemorrhage

Start date: September 2012
Phase: N/A
Study type: Observational

Traumatic brain injury is common cause of morbidity and mortality worldwide. Incidence and pattern of traumatic brain injury varies in developed and developing countries. Subarachnoid haemorrhage refers to blood in subarachnoid space that lies between arachnoid and piameninges, covering brain. It is often associated with concurrent intracranial injury component. Individuals at higher risk for tSAH are those who are at higher risk for blunt head trauma. This includes adolescents, low-income individuals, men, and individuals with a history of substance abuse. The investigators present study aims to investigate prognostic factors associated with the neurological outcome among patients of post traumatic SAH.

NCT ID: NCT02072343 Completed - Hemorrhage Clinical Trials

The Effect of 10 cm Catheter Mount on Malfunction of Capnometers Under the Conditions of Water

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

Capnometer has been used to assess the success of intubation and the quality of cardiopulmonary resuscitation. However, capnometers can malfunction under the conditions such as pulmonary edema and hemorrhage due to the vulnerability of capnometers for water. Investigators hypothesized that the use of 10cm catheter mount will reduce the malfunction of capnometers under the conditions of water.

NCT ID: NCT02064075 Completed - Clinical trials for Subarachnoid Hemorrhage

The Mortality and Changes in Quality of Life of Patients Suffering From SAH With Different Hydration Strategies

Start date: February 2013
Phase: Phase 4
Study type: Interventional

Purpose: - Vasospasm and secondary ischemia following subarachnoidal hemorrhage considerably affect the clinical outcome. The purpose of this study is to determine whether crystalloid (Lactated Ringer's solution) or colloid (hydroxyethyl starch) intravenous infusion is more effective in the treatment of subarachnoid hemorrhage (SAH) Treatment: - Patients are randomly divided into two groups. Depending on the blood pressure of the patients the members of the first group receive 15-50 ml/kg Lactated-Ringer's solution daily as part of the treatment, while the others 15 ml/kg Lactated-Ringer's and 15-50 ml/kg hydroxyethyl starch solution daily. Measurements: - Neurological status of patients will be determined by the NIH Stoke Scale Score and the Glasgow Coma Scale (GCS) on a daily basis. - The mid-term survival and quality of life are evaluated with Barthel Index and Glasgow Outcome Scale (GOS) 14 and 30 days following admission to our clinic. Hypothesis: -The prevalence of vasospasms, the mortality rate and the medium-term quality of life following subarachnoid hemorrhage is improved if patients are treated with intravenous colloid (hydroxyethyl starch) infusion compared to intravenous crystalloid infusion.

NCT ID: NCT02053922 Completed - Clinical trials for Postpartum Hemorrhage

The Use of Oxytocin, Carbetocin and Buccal Misoprostol in Patients Undergoing Elective Cesarean Section (CS)

Start date: December 2012
Phase: Phase 3
Study type: Interventional

The use of Oxytocin, Carbetocin and buccal misoprostol in patients undergoing elective Cesarean Section

NCT ID: NCT02047565 Completed - Bleeding Clinical Trials

A Two-part Study in Edoxaban-treated Healthy Subjects to Establish a Punch Biopsy Bleeding Model and to Evaluate the Effect of a 4-factor Prothrombin Complex Concentrate on Anticoagulation

Start date: October 2013
Phase: Phase 1
Study type: Interventional

This Phase 1 study consists of 2 parts. Part 1 will be an open-label, randomized, 2 treatment, 2-way crossover study. Part 2 will be a double-blind (Sponsor unblinded), randomized, placebo controlled, sequential descending prothrombin complex concentrate dose, 2 sequence, 2 period crossover study. In both parts of the study, the assessor of BD and BV will remain blinded. In Part 2 of the study, both the subject and the clinic staff involved in study conduct will be blinded (with the exception of the pharmacist or nurse who prepares the blinded individual treatments from open-label supplies). The study programmer and statistician will also be blinded to treatment assignment. The Sponsor will remain unblinded for both parts of the study.