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Epistaxis clinical trials

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NCT ID: NCT02127554 Completed - Clinical trials for Nosebleed (Epistaxis) - Posterior or Anterior

Long Term Results and Complications After Epistaxis Treatment

Start date: January 2014
Phase: N/A
Study type: Observational

The aim of this study is to find the most agreeable and in the long term most efficient treatment for epistaxis.

NCT ID: NCT01507480 Completed - Clinical trials for Telangiectasia, Hereditary Hemorrhagic

The ELLIPSE Study: A Phase-1 Study Evaluating the Tolerance of Bevacizumab Nasal Spray to Treat Epistaxis in Hereditary Hemorrhagic Telangiectasia

ELLIPSE
Start date: October 2011
Phase: Phase 1
Study type: Interventional

Antiangiogenic drugs, such as bevacizumab, are a new treatment strategy in Hereditary Hemorrhagic Telangiectasia (HHT). Its systemic administration in patients with HHT improves liver damage-related symptoms and epistaxis (cases reported and on-going study-ClinicalTrials.gov Identifier #NCT00843440-). To limit the systemic adverse effects of bevacizumab and to ease administration, a local administration seems suitable. A clinical case recently showed the benefits of bevacizumab nasal spray in these patients. Its results were confirmed in a characterization study on bevacizumab transport through porcine nasal mucosa (in press). It seems necessary to assess the tolerance and efficacy of bevacizumab nasal spray in humans for the treatment of epistaxis in HHT with a prospective phase 1 study. The primary objective of the study is to evaluate the tolerance of increasing doses of bevacizumab administered as a nasal spray in patients with HHT-related epistaxis. This phase-1, randomized, double-blind, placebo-controlled, monocentric study is to be carried out sequentially (dose escalation) on 5 groups of 8 patients. Each group is made up of 6 verum and 2 placebos.

NCT ID: NCT01485224 Completed - Epistaxis Clinical Trials

Efficacy of Thalidomide in the Treatment of Hereditary Hemorrhagic Telangiectasia

THALI-HHT
Start date: November 2011
Phase: Phase 2
Study type: Interventional

Hereditary hemorrhagic telangiectasia (HHT) (OMIM 187300 and 600376), also known as Rendu-Osler-Weber syndrome, is an autosomal dominant disease and has a prevalence between 1:5000 and 1:8000 in different populations. Clinically, the occurrence of mucocutaneous and gastrointestinal telangiectasias and of systemic arteriovenous malformations is commonly observed. Recurrent and severe epistaxis, due to the presence of telangiectasias in nasal mucosa, is the most common presentation of HHT, frequently leading to severe anemia requiring intravenous iron and blood transfusions. Although not life threatening, severe epistaxis has a great impact on quality of life in HHT patients and it represents the most important impediment in daily activities, that poses therapeutic challenge. Recently, angiogenesis has been implicated in the pathogenesis of HHT. Circulating concentrations of both TGF-beta and vascular endothelial growth factor (VEGF) are significantly elevated and therefore, anti-angiogenic substances may be effective in the treatment of vascular malformations in this disease. Thalidomide functions as a potent immunosuppressive and antiangiogenic agent. The aim of this study is to assess the clinical effects of thalidomide therapy on the severity of epistaxis in subjects with HHT who are refractory to standard therapies.

NCT ID: NCT01408732 Completed - Epistaxis Clinical Trials

Office-sclerotherapy for Epistaxis Due to Hereditary Hemorrhagic Telangiectasia

Start date: February 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to test a novel and tolerable office-based treatment method, sclerotherapy with sodium tetradecyl sulfate, for recurrent epistaxis (nosebleeds) related to Hereditary Hemorrhagic Telangiectasia (HHT) disease.

NCT ID: NCT01408030 Completed - Epistaxis Clinical Trials

North American Study of Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT)

NOSE
Start date: August 2011
Phase: Phase 2
Study type: Interventional

The purpose of the NOSE Study is to carefully examine the efficacy and safety of 3 nasal sprays (bevacizumab, estriol, and tranexamic acid), compared to placebo, for the treatment of HHT related nosebleeds.

NCT ID: NCT01402531 Completed - Clinical trials for Hereditary Hemorrhagic Telangiectasia (HHT)

Submucosal Bevacizumab for the Management of Recurrent Epistaxis in Patients With Hereditary Hemorrhagic Telangiectasia (HHT)

Start date: July 22, 2010
Phase: Phase 2
Study type: Interventional

This is a research study to find out more about the use of Avastin (proper chemical name is bevacizumab) in the treatment of epistaxis (nose bleeding) in patients with Hereditary Hemorrhagic Telangiectasia (HHT).

NCT ID: NCT01397695 Completed - Clinical trials for Hereditary Hemorrhagic Telangiectasia (HHT)

Topical Bevacizumab for the Management of Recurrent Epistaxis in Patients With Hereditary Hemorrhagic Telangiectasia (HHT)

Start date: June 2009
Phase: Phase 2
Study type: Interventional

Terence M. Davidson, MD is conducting a research study to find out more about the topical application of Avastin (proper chemical name is bevacizumab) in the treatment of epistaxis (nose bleeding) in patients with Hereditary Hemorrhagic Telangiectasia (HHT).

NCT ID: NCT01314274 Completed - Epistaxis Clinical Trials

Intranasal Submucosal Bevacizumab for Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT)

Start date: March 2011
Phase: Phase 2
Study type: Interventional

In a case series intranasal submucosal bevacizumab has been shown to reduce epistaxis in patients suffering from Hereditary Haemorrhagic Telangiectasia together with KTP Laser therapy. The aim of this study is to evaluate the effectiveness of submucosal intranasal bevacizumab compared to placebo in a randomized double blind trial setting.

NCT ID: NCT01098578 Completed - Epistaxis Clinical Trials

Floseal Treatment for Posterior Epistaxis Study

Start date: April 2010
Phase: N/A
Study type: Interventional

Effectiveness of Floseal for the treatment of posterior epistaxis.

NCT ID: NCT00863356 Completed - Epistaxis Clinical Trials

Trial of a Novel Chitosan Hemostatic Sealant in the Management of Complicated Epistaxis

Start date: March 2009
Phase: N/A
Study type: Interventional

Purpose: This study is a prospective clinical trial to investigate the efficacy of a chitosan-coated nasal packing (ChitoFlex® used in conjunction with the HemCon Nasal Plug) in the management of difficult spontaneous epistaxis and to evaluate its healing effect on nasal mucosa. The introduction of products that enhances hemostasis can have clinical advantages when associated with traditional nasal packing. These advantages include a better hemostatic control and the reduction of nasal packing duration. Furthermore, this study will help determine if there are any non-desirable effects that chitosan may have on the nasal cavity, such as the production of fibrosis and foreign body reaction.