Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
200 participants
OBSERVATIONAL
2025-12-01
2026-12-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Sepsis in ICU:Causes and Outcomes of Sepsis in Diabetics Versus Non Diabetics in Assiut University Hospital
NCT04015752
Sepsis in Respiratory Intensive Care Unit
NCT05240157
Blood Indices of Systemic Inflammation in Critically Ill Patients With Abdominal Sepsis
NCT06095830
Serum STREM and MNDA Mointoring in ICU
NCT02120521
Sepsis in ICU:Causes and Outcomes in Diabetics and Non Diabetics
NCT05914480
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patients with septic shock in the ICU
Blood sampling for thyroid and adrenal hormones
Blood sampling
Blood sampling for the hormones
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Blood sampling
Blood sampling for the hormones
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* admitted in ICU
Exclusion Criteria
2. Patients with previous endocrinal disorders.
3. Patients receiving corticosteroid or thyroid hormonal therapy.
4. Pregnancy or lactation.
5. Previous endocrinal gland surgery.
6. Individuals with pacing rhythms, bundle branch blocks (QRS interval \>120 ms),
18 Years
70 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Assiut University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Radwa mahmoud elsayed
principal investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Radwa m elsayed, MB
Role: PRINCIPAL_INVESTIGATOR
assuit university hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Radwa mahmoud
Asyut, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Assuit U Hospital
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
TAICU
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.