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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06285656
Other study ID # ASH-KG
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 1, 2024
Est. completion date October 3, 2024

Study information

Verified date February 2024
Source Ankara City Hospital Bilkent
Contact Hüseyin Fahri Martli
Phone +905301794699
Email fahri_martli@hotmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Postoperative bleeding is still an important concern after major abdominal surgery. Postoperative bleeding is the most important determinant of morbidity and death. It results in longer hospital stays, the necessity for extra radiological tests, interventional radiology treatments, and the possibility of reoperation. Early detection of postoperative bleeding reduces morbidity and mortality with appropriate intervention.Simultaneous arterial and venous blood gas measurements can be used to quickly identify the degree of bleeding and the need for replacement in serious trauma patients brought to the emergency room.Lactate levels, venous oxygen saturation, and the differential in partial pressure of carbon dioxide between arterial and venous blood can all be used to indicate the requirement for replacement, as demonstrated in several studies. The purpose of this study is to evaluate lactate levels, venous oxygen saturation, and arterial-venous partial pressure of carbon dioxide difference in blood gas analysis in order to assess the severity of bleeding in patients undergoing major abdominal surgery as early as possible and perform replacement as soon as possible.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date October 3, 2024
Est. primary completion date October 1, 2024
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with major abdominal surgery - Postoperative intensive care unit following - Accepting to participate in research Exclusion Criteria: - Age under 18 years old - Pregnant patients - Do not accept to participate of study

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ankara City Hospital Bilkent

Outcome

Type Measure Description Time frame Safety issue
Primary Eritrocyte replacement could we predict eritrocyte replacement at early postoperative period? 6 months
Secondary Postoperative Hemmorhagea Could we predict postoperative hemorrhage in the early postoperative period? 6 months
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