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Hemorrhage clinical trials

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NCT ID: NCT01837810 Recruiting - Clinical trials for Secondary Post Tonsillectomy Hemorrhage

Safety Study of Post Tonsillectomy Ibuprofen Use in Adults

Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if ibuprofen use after electrocautery tonsillectomy increases the post-tonsillectomy hemorrhage rate. Hypothesis: Use of ibuprofen does not increase the post-tonsillectomy hemorrhage rate. Primary outcome: Rate of tonsillar hemorrhage following adult tonsillectomy in those receiving narcotic pain medications plus ibuprofen compared to those receiving narcotics alone. Secondary outcome: Determine whether ibuprofen, a non-steroidal anti-inflammatory drug (NSAID), decreases post tonsillectomy pain, narcotic pain medication use, or cost of pain management.

NCT ID: NCT01837030 Withdrawn - Anemia Clinical Trials

Capsule Endoscopy Versus Conservative Therapy for Obscure Gastrointestinal Bleeding

Start date: March 2013
Phase: N/A
Study type: Interventional

This study is a single center prospective randomized control trial comparing the utility of performing capsule endoscopy compared to conservative management with oral iron therapy as the initial course of action in patients with non-severe obscure occult or obscure overt gastrointestinal (GI) bleeding. The investigators hypothesize that outcomes in patients with non-severe obscure GI bleeding who receive conservative therapy with oral iron will not differ to those on oral iron who undergo capsule endoscopy.

NCT ID: NCT01836848 Not yet recruiting - Clinical trials for Traumatic Brain Injury

Non-invasive Measuring of Cerebral Perfusion After Severe Brain Injury With Near-infrared-spectroscopy and ICG

Start date: June 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to show if it is possible to detect secondary ischemic events in patients with severe brain injury or cerebral haemorrhage with the help of non-invasive near-infrared spectroscopy (NIRS) by using the indocyanine green measuring of cerebral perfusion.

NCT ID: NCT01835067 Completed - Clinical trials for Exudative Macular Degeneration

Intravitreal tPA and C3F8 for the Treatment of Submacular Haemorrhage as a Complication of Neovascular AMD

TAPAS
Start date: September 2014
Phase: Phase 2/Phase 3
Study type: Interventional

This study will recruit patients who have recently had a submacular haemorrhage (bleed under the part of the retina responsible for detailed vision), as a complication of wet age-related macular degeneration (wet AMD). Wet AMD is a very common disease where abnormal blood vessels form under the retina and leak, causing a significant reduction in vision. The study will investigate treatment of the bleed with various combinations of the two drugs: tissue plasminogen activator (tPA) - designed to dissolve the blood clot; and perfluoropropane (C3F8) - designed to shift the blood clot away from the central part of the retina (the macula). tPA is a commonly used 'clot-buster' drug for the treatment of stroke. C3F8 is a gas commonly used in eye surgery. Patients recruited will be divided into four groups: control group that receive none of the above drugs; one group that receives only tPA; one group that receives only C3F8; and one group that receives both. All patients will receive the current gold standard treatment for wet AMD, ranibizumab (Lucentis®). The aim of the study is to improve vision in a condition, which left untreated, would cause severe visual loss.

NCT ID: NCT01834612 Completed - Blood Loss Clinical Trials

Evaluation of the Zynex Blood Volume Monitor in Healthy Adult Volunteers During a Blood Draw

Start date: January 7, 2013
Phase: Phase 1
Study type: Interventional

To determine if a manual blood loss can be detected using the non-invasive blood monitor.

NCT ID: NCT01832389 Completed - SAH Clinical Trials

Goal Directed Therapy After Aneurysmal Subarachnoid Haemorrhage

PiSAH
Start date: March 2013
Phase: N/A
Study type: Interventional

The objective of this study is to determine whether a goal-directed therapy can reduce the incidence of delayed cerebral ischaemia after aneurysmal subarachnoid haemorrhage.

NCT ID: NCT01827046 Completed - Clinical trials for Intracerebral Hemorrhage

Minimally Invasive Surgery Plus Rt-PA for ICH Evacuation Phase III

MISTIE-III
Start date: December 30, 2013
Phase: Phase 3
Study type: Interventional

A phase III, randomized, case-controlled, open-label, 500-subject clinical trial of minimally invasive surgery plus rt-PA in the treatment of intracerebral hemorrhage (ICH).

NCT ID: NCT01824043 Recruiting - Clinical trials for Diabetic Retinopathy

Use of Intravitreal Ranibizumab in the Treatment of Vitreous Hemorrhage

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

Primary Objective: To investigate the effectiveness of intravitreal applications of 0.5 mg Lucentis (ranibizumab) in patients with vitreous hemorrhage due to proliferative diabetic retinopathy. The primary endpoint for the study will be the mean change in best-corrected visual acuity (BCVA) from baseline to the mean level at Month 3. Secondary Objectives: 1. To assess any differences in mean change in BCVA over time; 2. To assess differences in vitreous transparency (amount of hemorrhage) with fundus angiography exam; 3. To assess any differences in retinopathy severity level according to the Early Treatment Diabetic Retinopathy Study; 4. To correlate the visual outcomes with serum glucose levels.

NCT ID: NCT01822600 Completed - Hypoalbuminemia Clinical Trials

The Therapeutic Role of Intravenous Albumin Administration for Peptic Ulcer Bleeding Patients With Hypoalbuminemia

Start date: January 2010
Phase: Phase 4
Study type: Interventional

To test whether intravenous albumin can decrease the rebleeding rate or shorten the duration of hospitalization in patients with peptic ulcer bleeding and hypoalbuminemia.

NCT ID: NCT01821326 Completed - Clinical trials for Gastrointestinal Bleeding

Risk Factors for Rebleeding in Patients With Obscure Gastrointestinal Bleeding

Start date: June 2002
Phase: N/A
Study type: Observational

The investigators investigated the rebleeding rate the risk factors for rebleeding after long-term follow-up (≥12 months) in patients who underwent capsule endoscopy for obscure gastrointestinal bleeding.