Epistaxis

7

Review clinical trials related to Epistaxis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Topical TOR-582 Treatment of Epistaxis in HHT

People with hereditary hemorrhagic telangiectasia (HHT) often experience frequent and severe nosebleeds that can disrupt daily life and lead to anemia, medical procedures, and reduced quality of life. This study is testing a new nasal ointment called TOR-582, which contains sirolimus, to determine whether it can be used safely when applied inside the nose. Adults with HHT and frequent nosebleeds will be invited to participate. Participants will first complete one week of observation without treatment, followed by up to 12 weeks of applying the study ointment inside each nostril twice daily. Different participants will receive different strengths of the ointment so researchers can identify the safest dose. During the study, participants will attend study visits, complete questionnaires about their nosebleeds and quality of life, keep a daily nosebleed diary, undergo nasal examinations, and have blood tests to monitor safety and medication levels. The information gained from this study will help determine whether this topical treatment can be safely studied further and will support the development of a new, less invasive option for managing nosebleeds in people with HHT.

Participants needed: 27
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Columbia UniversityUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Age 18 years or older at the time of consent. [+11]

Any medical contraindication to systemic sirolimus use. [+23]

Status: Not yet recruiting

Outcome of Hyaluronic Acid Gel Versus Petroleum Jelly in Treatment of Epistaxis

The aim of this study is to compare the efficacy of Hyaluronic Acid Gel with Petroleum Jelly in treatment of epistaxis.

Participants needed: 50
Trial details
Biological sex: AllType: InterventionalSponsor: Assiut UniversityUpdated: Apr 22, 2026
Eligibility criteria

Patients with anterior localized idiopathic epistaxis

Patients wit secondary epistaxis (posttraumatic, postoperative, tumoral). [+2]

Status: Not yet recruiting

The Efficacy of Local Application of B-sitosterol Versus Vasline in Cases of Idiopathic Epistaxis

Epistaxis, commonly known as nosebleed, is a frequent otorhinolaryngological complaint, affecting a large proportion of the population. Approximately 60% of individuals experience at least one episode during their lifetime, while around 6% require medical intervention'. The majority of cases are anterior in origin, arising from Kiesselbach's plexus in the anterior nasal septum(2) Idiopathic epistaxis refers to recurrent nasal bleeding without any identifiable local or systemic cause. (3) Factors such as mucosal dryness, minor trauma, inflammation, and environmental conditions can predispose the nasal mucosa to bleeding(4) Maintaining mucosal integrity and hydration is essential in preventing recurrence. Conservative management remains the first-line treatment for anterior epistaxis. Strategies include direct nasal compression, topical vasoconstrictors, nasal packing, and application of moisturizing agents(5) Petroleum jelly (Vaseline) is widely used as a topical agent to maintain hydration, protect the mucosa, and reduce crust formation, thereby minimizing the risk of further bleeding(6) B-sitosterol, a plant-derived phytosterol, has shown anti-inflammatory, immunomodulatory, and tissue-healing properties in several experimental and clinical studies'(7,8) Its anti-inflammatory activity may stabilize the nasal mucosa and enhance repair processes, suggesting a potential therapeutic rol in conditions like idiopathic epistaxis(9) Previous studies hav demonstrated B-sitosterol's efficacy in reducing mucosal inflammation and promoting healing in other mucosal tissues, although its use in ENT applications remains underexplored'(7,8) Considering these properties, B-sitosterol may represent a promising topical alternative to conventional moisturizers such as Vaseline for managing idiopathic epistaxis. This study aims to evaluate and compare the efficacy of local B-sitosterol versus Vaseline in reducing the frequency, duration, and severity of nosebleeds in affected patients.

Participants needed: 162
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Assiut UniversityUpdated: Apr 15, 2026
Eligibility criteria

Patients with recurrent idiopathic anterior epistaxis > = 2 episodes in last mon... [+2]

Patients on anticoagulants [+2]

Status: Recruiting

Comprehensive HHT Outcomes Registry of the United States (CHORUS)

The Comprehensive HHT Outcomes Registry of the United States (CHORUS) is an observational registry of patients diagnosed with Hereditary Hemorrhagic Telangiectasia (HHT). The purpose of this study is to better understand HHT, the symptoms and complications it causes, and the impact the disease has on people's lives. The investigators will collect long-term information about the participant, allowing us to understand how the disease changes over time, and what factors can influence those changes. Ultimately, this should help improve treatments for the disease. Another important goal of the study is to provide a way to contact people to participate in future clinical trials and other research. The registry will be a centralized resource for recruitment for clinical trials. People in the registry will not be obligated to join any of these additional studies, but if interested, can agree to be contacted if they may be eligible for a study. Participants will: * Be asked to provide permission to collect information from their medical records, including things like demographic information, diagnosis information, family history, test results, treatment information, symptoms, complications, lifestyle and other relevant medical information. * Be asked study-related questions by phone or at a clinic visit. * Be asked study-related questions every year after enrollment for up to 10 years or until the study ends. A member of the study team will communicate with participants by phone or at clinic visits to collect information regarding any changes to their health over the previous year/s including new test results, treatment information, symptoms, and complications from HHT.

Participants needed: 10,000
Trial details
Biological sex: AllType: ObservationalSponsor: Cure HHTUpdated: Jun 13, 2025Locations: 16Duration: 10 Years
Eligibility criteria

Diagnosed with HHT based on the Curacao diagnostic criteria or genetic testing. [+1]

Unable to provide informed consent or informed consent via a parent or legally a...

Status: Not yet recruiting

Usage of Orange Peel Extract in Management of Epistaxis

Efficacy of orange peel extract in treatment of epistaxis in children

Participants needed: 60
Trial details
Age: 5-15Biological sex: AllType: InterventionalSponsor: Minia UniversityUpdated: Feb 20, 2025
Eligibility criteria

children with anterior epistaxis from little's area

patient with nasal polyp. [+2]

Status: Not yet recruiting

Risk Factors of Epistaxis Recurrence in Adults

We study all patients admitted to the Emergency Department in the Institution between 01/2022 and 07/2023. The information about the recurrence of nose bleeding was searched on their medical file and by calling the patient to confirm ou get the information. Thus, several potentiel risk factors were studied. The relation between recurrence and those factors were studied at first individually and then all the significant ones were analyzed with a multivarious statistical test.

Participants needed: 145
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, GrenobleUpdated: Oct 24, 2024Locations: 1Duration: 1 Day
Eligibility criteria

Patient who is admitted at the emergency department between 01/2022 and 07/2023... [+1]

Opposition to be included [+1]

Status: Recruiting

Medico-economic Evaluation of Management Strategies for Severe Epistaxis

Current recommendations consider surgical ligation and supra-selective embolization as equivalent in terms of efficacy and there is no clear consensus to choose between one and the other technique. In the absence of medico-economic studies, these recommendations could not be based on any differences in efficiency between the two techniques. The management of patients with severe non-traumatic epistaxis remains controversial and varies according to the hospital and/or university centers. In practice, the use of one or the other technique depends on the habits of each reference center.

Participants needed: 180
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 29, 2023Locations: 1
Eligibility criteria

Patient with severe epistaxis who failed treatment with double tamponade for mor... [+4]

Patient with epistaxis secondary to facial and/or surgical trauma. [+10]