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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04210726
Other study ID # 001
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date March 2020
Est. completion date March 2021

Study information

Verified date July 2023
Source Batroussy, Rafik
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This Study evaluates the effectiveness of Hypertonic Saline Bath in reducing the Cancer nodules' size, number and SUVmax.


Description:

Many previous studies have shown that the Cancer cells are over-hydrated, and that Hyponatraemia exists in many cases of Cancer. The Cancer cell's viability depends on Angiogenesis and formation of blood vessels that carry water and nutrient to the rapidly-dividing Cancer cells. This study tests the hypothesis that disrupting the water content of blood could lead to increasing its Tonicity and hence withdrawing water from the Cancer cells by Osmosis, which can result in disrupting the growth of the Cancer cell itself. This disruption of Blood Water content can be achieved using Osmotic Pressure differential via immersing the whole body in Hypertonic Saline Solution for a certain amount of time, thus making the Blood more Hypertonic relative to the cells of the body and of the cancer, leading to water withdrawal from the cells of the body and of the cancer. While body's cells can sustain temporary dehydration, Cancer cells could be negatively affected.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date March 2021
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 5 Years to 80 Years
Eligibility Inclusion Criteria: - Patients with PET/CT scan-confirmed Cancer (any type, any location and any stage) who have poorly responded to at least one cycle of conventional and standard therapy (Chemotherapy, Radiation or Drug therapy) . - Age 5 to 80 years old - Life expectancy of at least 1 year - Can understand and read English - Lives in Calgary Alberta Exclusion Criteria: Patients with the following medical conditions will be excluded: 1. Kidney diseases 2. Dialysis 3. Fever 4. On Blood Thinners or with any Coagulation disorder 5. History of stroke 6. Hypernatraemia 7. Hypotension (Low Blood Pressure) 8. Hypovolemia/Dehydration 9. Tachycardia (Rapid Heart rate) 10. Epilepsy 11. Open wounds 12. Any medical condition that might cause the patient to lose consciousness 13. Participants who cannot tolerate thirst during the 30 minutes bath. 14. Participants who are not residents of Calgary Alberta Canada with a valid Alberta Health Card.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
25% Hypertonic Saline Bath
25% Sea Salt (mainly Sodium Chloride - NaCl) in Tap Water Immersion Bath (made by adding Sodium Chloride in the form of Sea Salt to Tap Water to a concentration of 25%).
Other:
0.9% Isotonic Saline Bath
0.9% Sea Salt (mainly Sodium Chloride - NaCl) in Tap Water Immersion Bath (made by adding Sodium Chloride in the form of Sea Salt to Tap Water to a concentration of 0.9%).

Locations

Country Name City State
Canada Rafik Batroussy Calgary Alberta

Sponsors (1)

Lead Sponsor Collaborator
Rafik Batroussy

Country where clinical trial is conducted

Canada, 

References & Publications (2)

Machado M, Salgado TM, Hadgraft J, Lane ME. The relationship between transepidermal water loss and skin permeability. Int J Pharm. 2010 Jan 15;384(1-2):73-7. doi: 10.1016/j.ijpharm.2009.09.044. Epub 2009 Sep 30. — View Citation

McIntyre GI. Cell hydration as the primary factor in carcinogenesis: A unifying concept. Med Hypotheses. 2006;66(3):518-26. doi: 10.1016/j.mehy.2005.09.022. Epub 2005 Nov 3. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Reduction in Tumors size Tumor responses are evaluated in terms of change in tumor size represented by the linear measurements of all targeted lesions. The Hypertonic Sea Salt Bath intervention will be considered effective if there is a statistically-significant reduction in Means of the measured Cancer Cells sizes/dimensions for the same nodules between the two groups using a One-Way ANOVA test. 6 month
Primary Reduction in Tumors lesions numbers Tumor responses are evaluated in terms of change in tumor lesions number. The Hypertonic Sea Salt Bath intervention will be considered effective if there is a statistically-significant reduction in Means of the Cancer lesions number for the same nodules between the two groups using a One-Way ANOVA test. 6 month
Primary Reduction in Tumors lesions SUVmax (FDG-Maximum Standardized Uptake Values) Tumor responses are evaluated in terms of change in tumor SUV max (FDG-Maximum Standardized Uptake Values). The Hypertonic Sea Salt Bath intervention will be considered effective if there is a statistically-significant reduction in Means of the measured Cancer lesions SUVmax values for the same nodules between the two groups using a One-Way ANOVA test. 6 month
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