Investigating the link between atmospheric pressure and gastrointestinal bleeding
The Effect of Atmospheric Pressure on Patients Presenting to the Emergency Department With Gastrointestinal Bleeding
This study is trying to see if changes in atmospheric pressure can affect the chances of people having upper gastrointestinal bleeding when they come to the emergency room.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 250 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Saglik Bilimleri Universitesi Academic / other |
| Locations | 1 site (Ankara, Yenimahalle) |
| Trial ID | NCT06515353 on ClinicalTrials.gov |
What this trial studies
This observational study aims to explore the relationship between atmospheric pressure and upper gastrointestinal bleeding (UGIB) in patients presenting to the emergency department. It will assess whether changes in atmospheric pressure can influence the occurrence of UGIB, which includes conditions like peptic ulcers and gastritis. The study will involve routine monitoring of patients for gastrointestinal bleeding without any additional invasive procedures. Data collected will be analyzed to identify any correlations between atmospheric pressure fluctuations and UGIB incidents.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18 and above who present to the emergency department with gastrointestinal bleeding complaints.
Not a fit: Patients under 18, pregnant individuals, or those with a history of trauma at the time of admission may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies for patients at risk of gastrointestinal bleeding based on weather conditions.
How similar studies have performed: While the relationship between atmospheric pressure and health outcomes is an emerging area of interest, this specific investigation into UGIB is novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion criteria: Patients aged 18 and above Patients presenting to the emergency department with complaints of gastrointestinal bleeding, whether active or resolved Patients willing to participate in the study Patients from central districts of Ankara Exclusion criteria: Patients under the age of 18 Pregnant individuals Patients with a history of trauma at the time of admission Patients declaring they are from a city other than Ankara
Where this trial is running
Ankara, Yenimahalle
- Etlik City Hospital — Ankara, Yenimahalle, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: gulsen akcay, ass. prof.
- Email: gulakcay@yahoo.com.tr
- Phone: +905052874949
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.