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
200 participants
OBSERVATIONAL
2023-04-01
2023-12-31
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.
Anesthesia-Related Peroperative Critical Events
NCT06426940
İntraoperative Awareness Under General Anesthesia
NCT04697732
The Effect of Anaesthesia Technique on Anxiety in Upper Extremity Surgery Patients
NCT06667596
Patient Satisfaction With Anesthesia Care
NCT02550587
Incidence of Chronic Pain After Video-Assisted Thoracic Surgery
NCT05187390
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.
OTHER
CROSS_SECTIONAL
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
A survey to assess anesthesiologists' secondary victim experience and quality of support resources.
cross-sectional descriptive questionnaire
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Volunteering to participate in the study
Exclusion Criteria
* Not volunteering to participate in the study
25 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Selcuk University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Faruk Cicekci
principal investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Selcuk University
Konya, , Turkey (Türkiye)
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.
Faruk Cicekci
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
farukcicekci7
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.