Digestive Cancer Clinical Trial
— PENDICOQOfficial title:
Improving the Quality of Life of Cancer Patients Through a Perioperative and Coordinated Nutrition and Physical Care Program.
NCT number | NCT03670199 |
Other study ID # | 6117 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | January 29, 2019 |
Est. completion date | April 28, 2024 |
Hospitalization, for cancer patients, exposes to a risk of undernutrition which has the effect of significantly increasing infections, pressure ulcers, muscle wasting, loss of autonomy, impaired function and delayed healing. All of these factors contribute to increase the length of stay in hospital, thus lengthening the spiral of undernutrition, which has serious consequences for the patient welbeing, health establishments and public health. Undernutrition has been the subject of many studies over the last twenty years, that outline that an adequate nutritional management exerts a direct effect on the reduction of comorbidities and duration of hospitalization. However, there are periods, in the preoperative course of care, where nutritional and phisical care are not realized in the current clinical practice whereas they could be done, for example, between the diagnosis and the consultation of anesthesia, between the anesthesia consultation and the surgical procedure and the end of hospitalization of the patient. Current management is usually limited to the period of hospitalization which tends to be reduced. This situation is reinforced by the absence of relays at home, dietary consultations being not reimbursed by French health insurance. Moreover, a preliminary survey, conducted in 2012 during the pre-operative outpatient anesthesia consultation, shows that 26% of patients are already clinically malnourished, with 16.5 % of them who have lost more than 10% of their weight.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | April 28, 2024 |
Est. primary completion date | April 28, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patient = 18 years old - Patient with Karnofsky index superior or equal to 60%. - Patient with cancer of the following digestive tract: peritoneal carcinoma, sarcoma, pancreas, rectum, esophagus, stomach diagnosed or under diagnosis - Patient admitted for a scheduled surgery at least 10 days after a preoperative consultation - Patient affiliated to a social health insurance scheme - Patient having dated and signed an informed consent - Patient having been informed of the results of the prior medical examination Exclusion Criteria: - Inhospital patients - Patient admitted in emergency - Impossibility of giving the patient information (alteration of patient's cognitive function) - Illiteracy or dyscalculia - Patients protected (guardianship, curatorship, safeguard of justice) - Pregnancy, breastfeeding - Subject in exclusion period (determined by a previous or ongoing study), - Patient included in another ongoing clinical trial - Patient with neuro-endocrine cancer - Patient reoperated for the same pathology |
Country | Name | City | State |
---|---|---|---|
France | Service de Médecine Interne et Nutrition, Hôpital de Hautepierre, Hôpitaux universitaires de Strasbourg | Strasbourg |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Strasbourg, France |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Variation of the Medical Outcome Study Short Form 36 score | Use of a scale for quality of life | Change in score at 30 days before surgery and 1 Day before hospital discharge | |
Secondary | Sarcopenia index measurement | Measure from routine preoperative Computerized Tomography scan | 30 days before surgery | |
Secondary | Satisfaction score of the Nutrimus tool | Use of a questionnaire | 6 months postoperative | |
Secondary | Ease of use of the Nutrimus tool | Use of a questionnaire | 6 months postoperative | |
Secondary | Measurement of the Medical Outcome Study Short Form 36 score | Use of a scale for quality of life | Change in score at 1 day before surgery, 1 day before the end of hospitalization, 1 Month, 3 Months and 6 Months post hospitalization | |
Secondary | Evaluation of nutritional parameters | Use of a notebook | Change in values measures at 30 days to 10 days, 1 day before surgery, 1 day before the end of hospitalization, 1 Month, 3 Months and 6 Months post hospitalization | |
Secondary | Evaluation of respiratory and functional capacities | Change in measures at 30 days to 10 days, 1 day before surgery, 1 day before the end of hospitalization, 1 Month, 3 Months and 6 Months post hospitalization | ||
Secondary | Pain assessment | Use of a visual analogue scale Measure of score from 0 to 10 | Change in score at 30 days to 10 days, 1 day before surgery, 1 day before the end of hospitalization, 1 Month, 3 Months and 6 Months post hospitalization | |
Secondary | Length hospitalization | Length (in days) between hospital admission and discharge | Duration (in days) of patient's hospitalization |
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