Red Cell Distribution Width and Lactate Albumin Ratio as Prognostic Markers for Mortality in Sepsis and Septic Shock
Launched by TANTA UNIVERSITY · Jun 18, 2023
Trial Information
Current as of June 20, 2025
Unknown status
Keywords
ClinConnect Summary
This clinical trial is looking at two specific tests, called red cell distribution width and lactate/albumin ratio, to see if they can help predict how likely patients with sepsis and septic shock are to survive. Sepsis is a serious condition that happens when the body has a strong reaction to an infection, and septic shock is a more severe form of sepsis where blood pressure drops dangerously low. By understanding how these tests can indicate a patient's prognosis, doctors hope to improve care for those affected by these life-threatening conditions.
To participate in this study, individuals need to be between 18 and 60 years old and diagnosed with sepsis or septic shock. However, there are some people who won't be able to join, such as those who have certain blood disorders, received a blood transfusion recently, or have serious liver or kidney issues. If eligible, participants will undergo the tests being studied, and their health outcomes will be monitored to gather valuable information that could help future patients. It's important to note that the trial is not yet recruiting participants, so more details will be available soon.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Age from 18 to 60 years old.
- • 2. Clinical criteria of sepsis
- • 3. Or clinical criteria of septic shock including sepsis with persisting hypotension requiring vasopressors to maintain mean arterial pressure \> 65 mmHg and having a serum lactate level \> 2 mmol/L despite adequate volume resuscitation.
- Exclusion Criteria:
- • 1. No informed consent.
- • 2. Patient with incomplete information and data.
- • 3. The patient who received blood transfusion within 90 days before emergency admission.
- • 4. The patients who are known to have long-term conditions causing anemia like sickle cell anemia, thalassemia, iron deficiency anemia.
- • 5. Malignancy and chemotherapy during the previous 90 days.
- • 6. Patients with either hepatic dysfunction, renal failure, having any disease in which albumin should be supplemented as liver cirrhosis with ascites, nephrotic syndrome and burns.
About Tanta University
Tanta University is a prestigious academic institution located in Egypt, dedicated to advancing medical research and education. As a clinical trial sponsor, Tanta University leverages its extensive resources and expertise to conduct innovative research initiatives aimed at improving health outcomes. The university collaborates with a network of healthcare professionals, researchers, and institutions to facilitate rigorous clinical trials across various medical disciplines. Committed to ethical standards and scientific integrity, Tanta University strives to contribute to the global body of knowledge while fostering the next generation of medical professionals.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Tanta, Elgharbia, Egypt
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported