6 patients with head and neck cancer and refeeding syndrome, 4 different of preparations of phosphate orally

6 patients with head and neck cancer without refeeding syndrome, 4 different of preparations of phosphate orally

Refeeding Syndrome

Cancer of the Head and Neck

phosphate orally

Clinic for Ear, Nose and Throat Surgery, Rigshospital

Absorption of Orally Ingested Phosphate in Refeeding Syndrome

Absorption of Orally Ingested Phosphate in Head and Neck Cancer Patients With and Without Refeeding Syndrome

measurements up till 4 hours after oral ingestion

Jens Rikardt Andersen

Associate Professor, MD, MPA

Spray dried blackcurrant powder dissolved in water

(sucrose, glucose, fructose, maltodextrin, malic acid, citric acid, vitamin C, artificial blackcurrant flavouring and low-nitrate water)

Vascular Stiffness

Inflammation

Beverage: Spray dried blackcurrant powder dissolved in water

Beverage: Placebo (sucrose, glucose, fructose, maltodextrin, malic acid, citric acid, vitamin C, artificial blackcurrant flavouring and low-nitrate water)

University of Reading

Anthocyanin-rich Blackcurrant and Vascular Function

Effects of an Anthocyanin-rich Blackcurrant Beverage on Cardiovascular Function

Professor Parveen Yaqoob, MA, DPhil, RNutr, FAfN

Professor Parveen Yaqoob

GlaxoSmithKline

Cyclophosphamide- Epirubicin 6 course regimen to be used with Jobelyn

Routine drugs for treatment of Breast Cancer used with Placebo

Haematological Abnormality

Jobelyn (dietary Supplement) to be used with Cyclophosphamide-Epirubicin6

Jobelyn + Cyclophosphamide-Epirubicin6

Routine drugs for the treatment of breast cancer to be used with Placebo

Placebo + Cyclophosphamide - Epirubicin 6

Lagos State University Teaching Hospital

Lagos State University

The Safety and Efficacy of Jobelyn in the Treatment of Breast Cancer Patients

A Prospective Phase II Randomized, Blinded Study to Demonstrate the Effectiveness of Jobelyn for the Treatment of Breast Cancer Patients.

Evaluation of the expression of activated natural killer cells CD3-CD56+CD69+ after treatment with Jobelyn

Subjects would use form Safety Fractor-36 to score aspects of well-being

Changes in levels of hematocrit after treatment with Jobelyn

Abiodun Popoola

CONSULTANT IN THE DEPARTMENT OF ONCOLOGY LASUTH

Subjects will take Capros supplement (1 capsule) twice a day for 12 weeks.The subjects then will have blood drawn seven times throughout the course of the study.

Subjects will take Capros supplement (1 capsule) twice a day for 12 weeks.The subjects then will have blood drawn seven times throughout the course of the study.
Capros dietary supplement: Study participants will have 2 to 3 baseline blood draws, 3 blood draws while taking Capros supplements and 2 wash out blood draws after finishing 12 weeks of Capros supplementation. Participants will attend 7 to 8 study visits (depending on number of baseline visits needed) and at each visit participants will have their blood drawn as well as height, weight, blood pressure, and pulse measured.

Capros Dietary Supplement

Sex: Female, Male

Region of Enrollment

BMI (Body Mass Index)

Blood Pressure Systolic

Height

Weight

Blood Pressure Diastolic

Blood lipid panel including HDL, LDL, total cholesterol. Looking at Baseline to 12 weeks on supplement with a two week washout period

Subjects will take Capros supplement (1 capsule) twice a day for 12 weeks.The subjects then will have blood drawn seven times throughout the course of the study.
Capros dietary supplement: Study participants will have 2 to 3 baseline blood draws (as needed), 3 blood draws while taking Capros supplements and 2 wash out blood draws after finishing 12 weeks of Capros supplementation. Participants will attend 7 to 8 study visits (depending on number of baseline visits needed) and at each visit participants will have their blood drawn as well as height, weight, blood pressure, and pulse measured.

Change From Baseline in Lipid Profile

High-Sensitivity C-reactive Protein analysis in blood. Looking at Baseline to 12 weeks on supplement with a two week washout period

Changes in High-Sensitivity C-reactive Protein

C-reactive protein in blood as measured in a standard hospital laboratory. 12 weeks on supplementation data presented.

C-reactive Protein

Adenosine Diphosphate (ADP), Arachidonic acid (AA), and Collagen (unsure about the specific type of collagen) agonists will be measured using optical platelet aggregometry. Looking at Baseline to 12 weeks on supplement with a two week washout period

Changes From Baseline in Platelet Aggregometry

Overall Study

Chandan K. Sen

Hyperlipidemia

Study participants will have 2 to 3 baseline blood draws, 3 blood draws while taking Capros supplements and 2 wash out blood draws after finishing 12 weeks of Capros supplementation. Participants will attend 7 to 8 study visits (depending on number of baseline visits needed) and at each visit participants will have their blood drawn as well as height, weight, blood pressure, and pulse measured.

Capros dietary supplement

The Ohio State University

Effect Of Capros Supplementation On Cardiovascular Disease Risk Factors In Humans

Chandan K Sen

Professor

Natreon, Inc.

Visual oral exam, followed by OraTest Rinse Staining Procedure

OraTest + Visual Exam

Primary efficacy parameters, ratio of sensitivity of OraTest® in combination with visual exam versus visual exam alone is the difference between the adjusted specificity for OraTest in combination with visual exam and the adjusted specificity for visual exam alone.
Reported ratio as percentage of patients with abnormalities (suspicious lesions) found upon visual exam of the mouth with and without OraTest® dye.

Ratio (Percentage) of Sensitivity of OraTest + Visual Exam Versus Sensitivity of Visual Exam Alone

Mark Chambers, MS, DMD / Professor

Head And Neck Cancer

Oropharynx Cancer

Two (2) scheduled visits for visual examination of mouth for abnormal lesions and glands in the neck.

Visual Examination

Two (2) scheduled visits for rinse staining: 2 teaspoons of OraTest for 20 seconds, then spit.

OraTest

U.T.M.D. Anderson Cancer Center

OraTest in Combination With Visual Examination and Visual Examination Alone

Evaluation of OraTest in Combination With Visual Examination in the Improved Detection of Oral Mucosal Lesions Suspicious of Serious Pathology in High-Risk Patients for the Purpose of Referral to the Health Care Professional Experienced in Oral Cancer: Phase III Clinical Trial Comparing the Sensitivity and Assessing the Specificity of OraTest in Combination With Visual Examination and Visual Examination Alone in Patients at High Risk as Defined by Age and Lifestyle Factors (ZIL-401)

ribes missouriense/neoplasms

Absorption of Orally Ingested Phosphate in Refeeding Syndrome

Anthocyanin-rich Blackcurrant and Vascular Function

The Safety and Efficacy of Jobelyn in the Treatment of Breast Cancer Patients

Effect Of Capros Supplementation On Cardiovascular Disease Risk Factors In Humans

OraTest in Combination With Visual Examination and Visual Examination Alone

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