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Atmospheric Pressure and Epistaxis Relationship

Influence of Atmospheric Pressure on Patients Presenting to the Emergency Department With Epistaxis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06531577
Enrollment
600
Registered
2024-08-01
Start date
2024-04-01
Completion date
2025-04-01
Last updated
2024-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atmospheric Pressure; Adverse Effect, Epistaxis Nosebleed

Keywords

atmospheric pressure, epistaxis, blood pressure

Brief summary

In this study, investigators aim to understand the relationship between changes in atmospheric pressure and blood pressure, and to investigate whether these changes have an impact on the etiology of epistaxis.

Detailed description

This study aims to investigate the potential effects of changes in atmospheric pressure on epistaxis and, if such effects exist, to review treatment adjustments based on weather forecasts for hypertensive patients to prevent potential hypertensive emergencies and enhance patient comfort. This research poses no risk to patients and is purely observational and clinical in nature. The study will be conducted prospectively over a period of 6 months at the Emergency Department of Ankara Etlik City Hospital, focusing on patients presenting with epistaxis.After initial evaluation upon presentation to the emergency department, patients will undergo routine emergency department monitoring for epistaxis, including physical examination, vital sign monitoring, evaluation of coagulation parameters, and hemoglobin levels. Apart from routine tests, no additional invasive or non-invasive procedures will be performed by us. Data obtained from patients and daily atmospheric pressure parameters will be evaluated and analyzed.

Interventions

None listed

Sponsors

Ankara Etlik City Hospital
CollaboratorOTHER_GOV
Saglik Bilimleri Universitesi
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

Patients aged 18 and above Presenting to the emergency department with complaints of epistaxis, whether active or resolved. Willing volunteers consenting to participate in the study. Residing in central districts of Ankara

Exclusion criteria

Patients under the age of 18. Pregnant individuals. Those with a history of maxillofacial surgery. Patients reporting a history of trauma at the time of admission. Patients stating they are from a city other than Ankara.

Design outcomes

Primary

MeasureTime frameDescription
epistaxis24 hoursnumber of the patients with epistaxis will be evaluated accoridng to atmospheric preesure and wheather conditions on daily basis

Countries

Turkey (Türkiye)

Contacts

Primary Contactgulsen akcay, ass. prof.
gulakcay@yahoo.com.tr+905052874949
Backup Contactmehmet ceylan, resident
mhmtcyln71mtf@gmail.com+905073046839

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026