Chronic Lymphocytic Leukemia Responds to Dermal Chelation
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ClinicalTrials.gov Identifier: NCT03495492 |
Recruitment Status : Unknown
Verified April 2018 by Optimum Health, Natural Healthcare Center.
Recruitment status was: Not yet recruiting
First Posted : April 12, 2018
Last Update Posted : April 12, 2018
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Sponsor:
Optimum Health, Natural Healthcare Center
Information provided by (Responsible Party):
Optimum Health, Natural Healthcare Center
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Brief Summary:
The purpose of this clinical trial is to identify 50 participants with Chronic Lymphocytic Leukemia (CLL) and follow their total white blood cell (WBC) counts and absolute lymphocyte counts after performing dermal chelation and administering nutritional therapy
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Chronic Lymphocytic Leukemia | Device: Dermal Chelation Dietary Supplement: Nutritional Therapy | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 50 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Intervention Model Description: | Clinical trials with a single arm |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Dermal Chelation Lowers White Blood Cell Count in Chronic Lymphocytic Leukemia |
Estimated Study Start Date : | December 1, 2018 |
Estimated Primary Completion Date : | March 1, 2019 |
Estimated Study Completion Date : | March 1, 2019 |
Resource links provided by the National Library of Medicine

MedlinePlus related topics:
Blood Count Tests
Chronic Lymphocytic Leukemia
Leukemia
Nutritional Support
Arm | Intervention/treatment |
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Experimental: Participants
Group receiving dermal chelation and nutritional therapy
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Device: Dermal Chelation
Dermal chelation with Aqua DetoxTM system for one or more hours one or more times each week. Dietary Supplement: Nutritional Therapy Vitamins and minerals that will be taken one or more times a day. |
Primary Outcome Measures :
- Serial Total White Blood Cell Count [ Time Frame: up to 12 months ]Total WBC counts taken on a regular interval.
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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Clinical diagnosis of Chronic Lymphocytic Leukemia and has a toxic heavy metal load
- Toxic heavy metal load
Exclusion Criteria:
- Pregnant
- Pacemaker implants
- Organ transplant recipients
- Psychotic episodes or epileptic seizures
No Contacts or Locations Provided
Additional Information:
Publications of Results:
Other Publications:
Publications of Results:
Other Publications:
Responsible Party: | Optimum Health, Natural Healthcare Center |
ClinicalTrials.gov Identifier: | NCT03495492 |
Other Study ID Numbers: |
DCCLL2018 |
First Posted: | April 12, 2018 Key Record Dates |
Last Update Posted: | April 12, 2018 |
Last Verified: | April 2018 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Product Manufactured in and Exported from the U.S.: | No |
Keywords provided by Optimum Health, Natural Healthcare Center:
Chronic Lymphocytic Leukemia CLL Dermal Chelation Nutritional Therapy |
Additional relevant MeSH terms:
Leukemia Leukemia, Lymphoid Leukemia, Lymphocytic, Chronic, B-Cell Neoplasms by Histologic Type Neoplasms |
Lymphoproliferative Disorders Lymphatic Diseases Immunoproliferative Disorders Immune System Diseases Leukemia, B-Cell |