Charité
Berlin, 10117, Germany
NCT Number: NCT01367067
The objective of the study is to search for possible predictors for claustrophobia during magnetic resonance (MR) imaging. A claustrophobic event shall be defined by an incomplete examination, or a complete examination that requires coping actions by the staff. Coping actions may consist of the administration of sedatives, prism glasses, an MR imaging test run with the patient, a pause, the prone position, an escort in the scanner room, and supportive communication. The investigators hypothesize that there is a difference between patients with and without events in their scores on the Claustrophobia Questionnaire and several further psychometric questions. Other factors may also favour events like patient characteristics, examined region, duration of the examination and scanner type. Therefore, predictors could identify patients who are likely to experience claustrophobia during MR imaging so that they can receive the appropriate support by the staff to complete their examination. Thus a larger patient population could benefit from MR imaging.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Berlin, 10117, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Up to 5 min after the end of the MR
Time frame: Up to 5 min after the end of the MR
Time frame: Up to 5 min after the end of the MR
Charite University, Berlin, Germany
Other
Prediction of Claustrophobia During MR Imaging: An Observational 18-Months Single Center Study
Acronym: CLAUSTRO II
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.
Published trials that share one or more normalized conditions with this study.
NCT03384849
Anxiety, Anxiety Disorders
Warsaw, Poland
View Trial DetailsNCT02926352
Anxiety Disorders, Claustrophobia
Austin, Texas, United States
View Trial DetailsNCT04520100
Anxiety, Anxiety Disorders
Aurora, Colorado, United States
View Trial DetailsNCT00715806
Anxiety Disorders, Claustrophobia
Berlin, State of Berlin, Germany
View Trial Details