Last updated: February 7, 2023
Sponsor: The Christie NHS Foundation Trust
Overall Status: Active - Recruiting
Phase
N/A
Condition
Esophageal Cancer
Gastric Cancer
Anorexia
Treatment
N/AClinical Study ID
NCT04791254
CFTSp141
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Inclusion criteria: Cohort A
- Patients with stage IV gastric or GOJ adenocarcinoma or locally advancednon-resectable adenocarcinoma
- Histologically proven adenocarcinoma, squamous cell carcinoma or poorlydifferentiated carcinoma
- Patients should be chemotherapy or immune therapy naïve (for their currentdiagnosis).
- Patient must be 18 years of age or above.
- Patient must be able to understand the study information given to them and bewilling to give consent for trial participation.
- Patients should be commencing a course of palliative chemotherapy treatment withthe upper GI team at the Christie Hospital In addition the above patients enrolled in cohort B must meet the following criteria Inclusion criteria: Cohort B
- Be physically able to perform moderate exercise (to their own tolerance) on a stationarybicycle or treadmill In addition to the above patients in cohort C must meet the following criteria Inclusion Criteria: Cohort C
- Histologically proven adenocarcinoma or poorly differentiated carcinoma
- Patients should be chemotherapy or immune therapy naïve.
- Patients must be able and willing to fast for 8-10 hours. 4 5.1 Patients in theanorexic group must have completed the FAACT AC/S questionnaire and scored ≤24 intotal score and ≤ 2 in the appetite specific question.
5.2 For inclusion in the non-anorexic group patients must have completed the FAACT AC/Squestionnaire; the total score should be > 37 and ≥3 for the appetite specific question. Inclusion criteria: Cohort D - healthy controls
- Participants must be 18 years of age or above.
- Participants must be able and willing to fast for 8-10 hours.
- Participants must be able to understand the study information given to them and bewilling to give consent for trial participation.
- Participants must have completed the FAACT AC/S questionnaire and scored ≤24 in totalscore and ≤ 2 in the appetite specific question, for the anorexic group. For inclusionin the non-anorexic group the total score should be > 37 and ≥3 for the appetitespecific question.
Exclusion
Exclusion Criteria:
- Participants are excluded from the study if any of the following criteria apply: Exclusion criteria Cohort A:
- Patients unable to give informed consent
- Patients not undergoing systemic anti-cancer treatment at The Christie hospital, forexample patients not deemed fit enough for treatment, patients having alternativetreatments such as radiotherapy or surgery, or patients referred for 2nd opinions. Exclusion criteria Cohort B:
- Recent myocardial infarction or stroke
- Recent abdominal, eye or thoracic surgery
- A recent respiratory tract infection (within 3 weeks)
- Any chest pain on the day of the test
- A positive COVID-19 test Exclusion Criteria Cohort C & D : all patients and healthy volunteers
- Symptoms of dysphagia of any cause, oesophageal or gastric obstruction (assessed viamedical history/O'Rourke score). Patients with O'Rourke score ≥2 will be excluded.
- Presence of oesophageal stent or any other kind of feeding aid (nasogastric tube,nasoduodenal tube, gastrostomy, jejunostomy)
- Presence of brain metastases or any kind of brain tumor including benign pituitaryadenomas.
- Histological diagnosis of neuroendocrine tumor, or mixed tumor.
- Previous gastro-duodenal surgery.
- History of Inflammatory Bowel Disease (Ulcerative colitis, Crohn's disease).
- History of Coeliac disease.
- History of endocrine disease (Diabetes mellitus, Thyroid disease, Cushing's)
- Significant past or present eating disorder e.g. anorexia nervosa, bulimia nervosa.
- Current active infection (general or intestinal).
- Chronic use of immunomodulatory drugs (steroids, immunosuppressant drugs, recent useof corticosteroids would require a two week washout period prior to studyassessments).
- Chronic use of NSAIDS or aspirin. (Periodic use can be accepted).
- Patients with pacemakers. (Contraindication for BIA).
- Allergy to any of the ingredients of the meal test or unwillingness to consume theparticular meal (Heinz Chicken soup or Heinz Mushroom soup).
Study Design
Total Participants: 450
Study Start date:
July 15, 2021
Estimated Completion Date:
April 30, 2026
Study Description
Connect with a study center
The Christie NHS Foundation Trust
Manchester, M20 4BX
United KingdomActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.