- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03221920
Very Low Carbohydrate Diet Effects to GPS, Serum Lactate and TNF Alpha on Colorectal Cancer
July 28, 2017 updated by: Dr. Soetomo General Hospital
Effect of Very Low Carbohydrate Diet to Glasgow Prognostic Score, Serum Lactate and TNF Alpha on Colorectal Cancer Patients With Best Supportive Care
This study examine the effects of very low carbohydrate diet (in which the calories requirements are mostly from fat) to the level of systemic inflammation (measured by Glasgow Prognostic Score), serum lactate and TNF Alpha levels
Study Overview
Status
Unknown
Intervention / Treatment
Detailed Description
This study examine the effects of very low carbohydrate diet (in which the calories requirements are mostly from fat) to the level of systemic inflammation (measured by Glasgow Prognostic Score), serum lactate and TNF Alpha levels.
The subjects are colorectal adenocarcinoma patients who were decided by experts to be managed by best supportive care.
These patients are not deemed to be suitable for surgical intervention , chemotherapy or radiotherapy anymore.
The main treatment is supportive.
We would like to examined the effect of very low carbohydrate diet on these patients, in which theoretically tumtor cells of the colorectal adenocarcinoma needed glucose to replicate and increases the systemic inflammation response.
Study Type
Interventional
Enrollment (Anticipated)
26
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Vicky S Budipramana, PhD
- Phone Number: 0811315812
- Email: vickysbudi@gmail.com
Study Contact Backup
- Name: Fransiscus Arifin, MD
- Email: farifin@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Diagnosed as colorectal adenocarcinoma pathologically
- Decided by a digestive surgery consultant to be managed with best supportive care
- More than 17 years old and capable of making informed consent
- Karnofsky score > 50% or ECOG performance status <=2
- No clinical signs of infection, with one or more of these criteria : fever, leukocytosis, local sign of infection (eg.abscess,ulcer)
- AST < 2 times normal limit
- ALT < 2 times normal limit
- Serum Creatinine < 1,5 times normal limit
- Not pregnant (for women)
- Able to understand and willing participate and to sign informed consent form
- No Diabetes Mellitus
- No fat intolerance
- No severe malnutrition or cancer cachexia
Exclusion Criteria:
- Patient is still on other therapy for the tumour
- Patient with coexisting diseases which prohibits the patient to follow the study protocols
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Very Low Carbohydrate Diet
The patient will be evaluated for baseline clinical and laboratory values, and counselled on very low carbohydrate diet.
|
1 : 4 ratio of carbohydrate to fat of the total daily calories intake
|
No Intervention: Control
The patient will be evaluated for baseline clinical and laboratory values, and counselled on normal healthy .
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Glasgow Prognostic Score
Time Frame: Change of baseline Glasgow Prognostic Score on day 21
|
A score to evaluate systemic inflammation response
|
Change of baseline Glasgow Prognostic Score on day 21
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Serum Lactate
Time Frame: Change of baseline Serum Lactate on day 21
|
Lactate level in blood serum
|
Change of baseline Serum Lactate on day 21
|
TNF Alpha
Time Frame: Change of baseline TNF Alpha serum level on day 21
|
Level of Tumor Necrosis Factor Alpha in the blood serum
|
Change of baseline TNF Alpha serum level on day 21
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Vicky S Budipramana, PhD, RS Dr Sutomo
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Sethi G, Sung B, Aggarwal BB. TNF: a master switch for inflammation to cancer. Front Biosci. 2008 May 1;13:5094-107. doi: 10.2741/3066.
- Allen BG, Bhatia SK, Anderson CM, Eichenberger-Gilmore JM, Sibenaller ZA, Mapuskar KA, Schoenfeld JD, Buatti JM, Spitz DR, Fath MA. Ketogenic diets as an adjuvant cancer therapy: History and potential mechanism. Redox Biol. 2014;2:963-70. doi: 10.1016/j.redox.2014.08.002. Epub 2014 Aug 7.
- Walenta S, Voelxen NF, Mueller-Klieser W. Lactate-An Integrative Mirror of Cancer Metabolism. Recent Results Cancer Res. 2016;207:23-37. doi: 10.1007/978-3-319-42118-6_2.
- San-Millan I, Brooks GA. Reexamining cancer metabolism: lactate production for carcinogenesis could be the purpose and explanation of the Warburg Effect. Carcinogenesis. 2017 Feb 1;38(2):119-133. doi: 10.1093/carcin/bgw127.
- Lasry A, Zinger A, Ben-Neriah Y. Inflammatory networks underlying colorectal cancer. Nat Immunol. 2016 Mar;17(3):230-40. doi: 10.1038/ni.3384.
- Seyfried TN, Flores RE, Poff AM, D'Agostino DP. Cancer as a metabolic disease: implications for novel therapeutics. Carcinogenesis. 2014 Mar;35(3):515-27. doi: 10.1093/carcin/bgt480. Epub 2013 Dec 16.
- Venetsanou K, Kaldis V, Kouzanidis N, Papazacharias Ch, Paraskevopoulos J, Baltopoulos G. Measurement of tumour necrosis factor receptors for immune response in colon cancer patients. Clin Exp Med. 2012 Dec;12(4):225-31. doi: 10.1007/s10238-011-0162-5. Epub 2011 Nov 1.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
August 5, 2017
Primary Completion (Anticipated)
August 30, 2017
Study Completion (Anticipated)
August 30, 2017
Study Registration Dates
First Submitted
July 16, 2017
First Submitted That Met QC Criteria
July 17, 2017
First Posted (Actual)
July 19, 2017
Study Record Updates
Last Update Posted (Actual)
August 1, 2017
Last Update Submitted That Met QC Criteria
July 28, 2017
Last Verified
July 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DrSoetomoGH
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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