Clinical Trials Directory

Trials / Unknown

UnknownNCT03575416

Cancer Anesthesia and Frailty

Prevalence of Multi-morbid Frailty in a Cohort of Subjects Undergoing Cancer Related Surgery

Status
Unknown
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
Fondazione IRCCS Istituto Nazionale dei Tumori, Milano · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Subjects undergoing cancer related surgery at the Fondazione IRCCS Istituto Nazionale dei Tumori - Milano will be consecutively recruited. Data regarding presence of co-morbidities, frailty, cancer staging, and inflammatory status (CRP protein measurement) will be collected preoperatively. Intra-operative data collection will comprehend type and duration of surgery, kind of anesthesia, complications. In-hospital mortality will be considered as the primary endpoint, while secondary outcome measures will be duration of hospital stay and admission to intensive care.

Detailed description

A prospective data collection of pre-intra and postoperative variables will be collected in a cohort of subjects undergoing cancer relate surgery at the Fondazione IRCCS Istituto Nazionale dei Tumori, Milano. BEFORE SURGERY Subjects will be stratified before surgery according to the following three main clusters: 1) Systemic inflammation: baseline levels of C Reactive Protein; 2) Cancer staging: TNM will be taken into account, together with the type of cancer, previous radio or chemo therapy, and planned/performed surgical procedure; 3) Frailty: subjects will be stratified according to their overall status, taking into account elements of frailty. Co-existing diseases such as diabetes, hypertension, cardiac heart failure, acute myocardial infarction, chronic obstructive disease/asthma, kidney or liver disease (past or present) will be considered. Functional status will be assessed by means of ASA, ECOG status and Possum scores. Frailty will be explored using the mFI and G8 score, the WHO scale, and considering age. Absolute BMI and loss of weight will be used to assess malnutrition. DURING SURGERY Duration and type of surgery, kind of anesthesia and intra-operative complications will be considered. AFTER SURGERY Hospital mortality, length of stay, and admission to intensive care will be considered as outcome measures. Major complications, such as myocardial infarction, arrhythmia, cardio circulatory arrest, shock, stroke, pulmonary embolism, kidney failure, delirium, pneumonia or SSI will also be considered.

Conditions

Timeline

Start date
2018-07-03
Primary completion
2018-09-01
Completion
2018-11-01
First posted
2018-07-02
Last updated
2018-07-11

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT03575416. Inclusion in this directory is not an endorsement.