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.
UNKNOWN
124 participants
OBSERVATIONAL
2019-02-06
2019-05-31
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.
Physiological Data Analysis of Patients Undergoing Anesthesia for Liver Transplantation
NCT03694301
Ultrasound Airway Examination as a Tool for Detection of Difficult Intubation in Adult Patients
NCT06700265
Evaluation of Complications in Airway Management
NCT03550326
Continuous and Discontinuous Determination of Propofol Concentration in Breathing Gas
NCT00532402
Risk Factors For Postoperative Respiratory Complications After Anesthesia
NCT01871051
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
RETROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Collection of data
The investigators will retrieve retrospectively the medical record of donors who underwent hepatic lobectomy for liver transplantation
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Free of chronic disease or
* Previous major abdominal surgery,
* Body mass index (BMI) \<28,
* ABO blood group identical to recipients and
* Negative for hepatitis B, C and human immunodeficiency viruses (HIV).
Exclusion Criteria
* BMI\>28,
* Psychiatric or mental retardation,
* pregnant and nursing women or
* Patients with significant laboratory abnormalities
20 Years
50 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ain Shams University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mohammed Sayed Shorbagy
Lecturer of Anesthesia
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ain Shams University hospitals
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
FAMSU R37/2018
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.