UPNA
Pamplona, Navarre, 31008, Spain
NCT Number: NCT03205384
Morbimortality in older patients undergoing abdominal surgery.
Looking for future studies?
Notify Me65 year–110 year
All sexes
Observational
Pamplona, Navarre, 31008, Spain
The aim of this study is to validate the modified CriSTAL tool for 30 mortality in elderly patients undergoing urgent abdominal surgery. To provide a new tool that could be used in conjunction with clinical judgment to aid in decision-making.
The second objective of our study was to assess the quality of life, frailty, functional status and nutritional status in elderly patients that survive six months after an urgent abdominal surgery.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 6 months
to measure performance in activities of daily living
Time frame: 1 year
Morbimortality using Clavien-Dindo classification
Time frame: 6 months
To measure frailty
Hospital of Navarra
Other
Analysis of Morbimortality and Functional Status in Older Patients(>65 Years Old) Undergoing Urgent Abdominal Surgery Using CRISTAL Score Modify
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.
NCT04293653
Digestive System Diseases, Frail Elderly Syndrome
Bergen, Norway
View Trial DetailsNCT04176432
Abdomen, Acute, Abdominal Pain
View Trial DetailsNCT03949439
Arterial Occlusive Diseases, Arteriosclerosis
São Paulo, Brazil
View Trial DetailsNCT04221295
Disability Physical, Frailty
Ottawa, Ontario, Canada
View Trial Details