Fethi Sekin City Hospital
Elâzığ, Elaziğ, Turkey (Türkiye)
Location status: Recruiting
NCT Number: NCT07435805
The Coronavirus Disease 2019 (COVID-19) pandemic has resulted in persistent health problems in a significant proportion of individuals after recovery from the acute infection. These long-term manifestations, commonly referred to as post-COVID-19 condition or long COVID, may involve respiratory, cardiovascular, neurological, psychological, and general health domains. Understanding these sequelae is particularly important in patients undergoing preoperative anesthesia evaluation, as residual symptoms may influence perioperative risk assessment and clinical decision-making. This cross-sectional observational study aims to evaluate the long-term clinical and health effects of previous COVID-19 infection in adult patients presenting to the preoperative anesthesia clinic. Patients aged 18 years and older who report a history of confirmed COVID-19 infection will be included. Clinical data related to the acute infection period (disease severity, hospitalization, intensive care unit (ICU) admission, oxygen therapy, and radiological findings) will be retrospectively obtained from hospital records. At the time of preoperative assessment, participants will complete a structured post-COVID-19 clinical questionnaire to evaluate persistent symptoms across multiple organ systems. The study seeks to determine the prevalence and characteristics of long-term post-COVID-19 symptoms and to explore potential associations between acute disease severity and ongoing health complaints. No additional medical intervention will be performed as part of this research.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Elâzığ, Elaziğ, Turkey (Türkiye)
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Presentation to the preoperative anesthesia clinic
Self-reported history of laboratory-confirmed COVID-19 infection
Ability to provide informed consent
Willingness to complete the post-COVID clinical questionnaire
Exclusion criteria
No history of COVID-19 infection
Refusal to participate or incomplete questionnaire
Cognitive impairment or communication difficulties preventing reliable data collection
Structured post-COVID symptom questionnaire and retrospective clinical data review performed at the time of preoperative anesthesia evaluation. No therapeutic intervention is applied.
Time frame: At the time of preoperative anesthesia assessment
Assessment of respiratory, cardiovascular, neurological, psychological, and general health symptoms using a structured post-COVID clinical questionnaire administered during preoperative anesthesia evaluation.
Contact information is provided by the study sponsor or research team.
Elazıg Fethi Sekin Sehir Hastanesi
Other
Long-Term Clinical and Health Effects of Previous Coronavirus Disease 2019 (COVID-19) in Patients Presenting for Preoperative Anesthesia Evaluation
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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