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The Weekend Effect and Its Possible Influence on the Prognosis of Patients With Non-varicose Upper Gastrointestinal Bleeding

Observational Study About the Weekend Effect and Its Possible Influence on the Prognosis of Patients With Non-varicose Gastrointestinal Bleeding

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04296435
Enrollment
1320
Registered
2020-03-05
Start date
2019-10-28
Completion date
2021-12-31
Last updated
2020-03-05

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

Conditions

Acute Upper Gastrointestinal Hemorrhage

Keywords

Weekend effect, non-varicose upper gastrointestinal bleeding

Brief summary

The hypothesis is that the mortality of patients with non-varicose upper gastrointestinal bleeding after performing early gastroscopy who are admitted on weekends and night hours is higher than those admitted on weekdays or during daytime hours.

Detailed description

The aim of the study is to evaluate the impact of the schedule (day or night) and the day of admission (working or weekend / night) on the mortality of patients with non-varicose upper gastrointestinal bleeding after performing an early gastroscopy. A retrospective observational study will be carried out in patients admitted to the bleeding unit of the Santa Creu I Sant Pau Hospital, where we observed hospital mortality and 30 days after performing an early gastroscopy, the duration of admission, signs of hemorrhagic activity in a period of less than 12 h. After early gastroscopy and types of endoscopic treatments, data will be collected by reviewing medical records. The number of patients expected to be included in this study is 1320 patients. Patients will be included the day they enter the bleeding unit for an early gastroscopy.

Interventions

None listed

Sponsors

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients older than 18 years. * Patients admitted to the Bleeding Unit with a diagnosis of upper gastrointestinal bleeding. * Patients who have undergone an early endoscopy to determine the source of bleeding. * In case of readmissions during the study period, we consider only the admission closest to his death or discharge.

Exclusion criteria

* Patients diagnosed with gastrointestinal bleeding varicose. * Patients who present with gastrointestinal bleeding and did not perform early gastroscopy (during the first 24 hours) * Patients admitted for different medical conditions, who developed upper gastrointestinal bleeding during the course of hospital stay.

Design outcomes

Primary

MeasureTime frameDescription
MortalityDuring the years 2017 and 2018In-hospital mortality and at 30 days after early gastroscopy will be assessed through clinical history observation, within the study period

Secondary

MeasureTime frameDescription
Entry DurationDuring the years 2017 and 2018The time between admission and discharge
Signs of bleeding activity in a period of less than 12 h. post gastroscopy early.During the years 2017 and 2018It will be evaluated using the Rockall scale
Type of endoscopic treatmentsDuring the years 2017 and 2018Hemostasis can be performed by applying different techniques or a combination of them

Countries

Spain

Contacts

Primary ContactLuzdivina Perez Garcia
Lperez@santpau.cat699940025

Outcome results

None listed

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