High dose Intravenous Vitamin C therapy
The anti-cancerous effect of high dose IV vitamin C therapy is through a mechanism whereby the vitamin C (ascorbate) is converted to hydrogen peroxide. Hydrogen peroxide generates an oxidative stress that preferentially targets cancer cells. Normal cells can neutralize hydrogen peroxide, making high dose vitamin C infusions selectively toxic to only cancer cells.
Unlike many anti-cancer treatments, high dose IV vitamin C has very few negative side effects. High dose vitamin C has been recognized by the National Cancer Institute (NCI), a part of the National Institutes of Health (NIH), as having beneficial effects in cancer management, and is currently being studied as a new adjunct to prevent cancer recurrence after surgery. Treatments are given by slow intravenous infusion, in increasing amounts of 30g, 60g or 90g per treatment, alongside other vitamins.
Treatment flow
Depending on the patient’s condition, the high dose IV vitamin C solution consists of a 500ml solution of vitamin C, alongside various other vitamins, minerals, alpha lipoic acid, etc., and is infused over approximately 60 to 90 minutes. The treatment is usually given once or twice a week for a course of 3 months to assess the effects of the treatment.
After the initial consultation, we will suggest a schedule of treatment frequency and time frame.
Side Effects
While there are no serious side effects, the following symptoms may occur:
- Pain at the intravenous injection site
→ Symptoms may be relieved by slowing down the infusion rate. - Feelings of thirst
→This is due to the diuretic action of the infusion. You can replenish your intake of water during the infusion. - Hypoglycemia
→Vitamin C has a chemical structure that is similar to glucose, and thus insulin may be secreted in response to the infusion. In rare instances, this may lead to hypoglycemia, and patients should try not to be in a fasted state during treatment.
Contraindications to treatment
- Patients with poor kidney function or are on dialysis
- Patients with poor nutritional status
- Patients with dehydration
- Patients with dialysis
- Patients with G6PD deficiency
Chelation Therapy
Chelation therapy is a treatment method in which a formula containing vitamins, minerals, and a chelating agent EDTA (ethylenediamine tetraacetic acid) is given intravenously.
In the early 1950s, chelation was used to treat heavy metal poisoning, as it binds and aids in the excretion of harmful toxins in the body, such as lead, mercury, and arsenic. In recent years, chelation therapy has been used to treat arteriosclerosis in the whole body, as it removes calcium from atherosclerotic plaques and improves heart function.
Symptoms and conditions that are targeted for chelation therapy in order to improve cellular functions and biological enzyme systems include: overall health promotion, anti-aging, angina pectoris, arteriosclerosis, intractable ulcers, hypertension, diabetes, arthritis, scleroderma, and cancer treatment.
Treatment flow
The chelation therapy consists of a 600ml solution containing vitamins, minerals, vitamins and EDTA (ethylenediamine tetraacetic acid) that is infused intravenously over a period of approximately 60-90 minutes.
After the initial consultation, we will suggest a schedule of treatment frequency and time frame.
Side Effects
While there are no serious side effects, occasionally symptoms such as pain at the intravenous injection site may occur. This is relieved by slowing down the infusion rate. Rarely, symptoms such as hypoglycemia, hypocalcemia, malaise or fatigue may occur. These symptoms are considered to be secondary phenomena caused by the excretion of harmful substances, vitamins or minerals through the kidneys. Supplemental hydration, vitamin administration, and nutritional guidance is provided as needed.
Contraindications to treatment
- Patients with kidney failure
- Women who are pregnant
Ozone Therapy
Ozone therapy is a treatment in which ozone gas (O3) is mixed with the patient’s blood and then returned to the body (ozonated autohemotherapy) in order to improve the body’s intake and use of oxygen and to activate the immune system. Ozone has high bactericidal and germicidal effects, and studies have shown that it induces cytokines produced by immune cells and increases the number of active monocytes and lymphocytes. When used in combination with cellular cancer immunotherapy, it not only helps to create an unfavorable environment for tumor cells, but also exerts a synergistic effect on immune cell activation and immune enhancement.
In Europe, ozone therapy is used to treat infections, poor wound healing, poor circulation, degenerative diseases, multiple skin conditions, rheumatic and allergic conditions, immune deficiencies, and as an adjunct to cancer treatments.
Treatment flow
Approximately 150ml of venous blood is withdrawn into a reservoir vessel, and 40 μ/ml of ozone gas is added to the reservoir and is dissolved in the blood. Once the ozone is incorporated, the mixture is then re-transfused into the body using the same intravenous route. This procedure is completed in under 30 minutes.
Side Effects
When ozone therapy was initially developed, vinyl transfusion bags were used as blood reservoirs, causing some side effects such as allergies. Currently, however, special non-reactive reservoirs are used, and no side effects have been reported.
Contraindications to treatment
- Patients with G6PD deficiency
- Women who are pregnant
- Patients who are being treated with ACE inhibitors
- Patients with hyperthyroidism
- Patients with thrombocytopenia
- Patients with severe vascular disease
- Patients who are allergic to ozone
Placenta Therapy
Placenta therapy uses an ethical drug manufactured from human placental extract in Japan (Laennec). The placenta, which supports fetal growth and development, is rich in amino acids, vitamins, nutrients, cytokines, growth factors, and other biologically active compounds. The pharmacological effects are based on the bioactive ingredients from the placental extract and is administered by subcutaneous or intramuscular injection.
Placenta extract has a variety of biological and therapeutic effects, including improvement of metabolism, promoting the balance of autonomic nerves and hormonal balance, and increasing immunity and resistance to disease. Not only is this indicated as a drug for chronic hepatic disease and used for gastrointestinal ulcers, as well as the symptomatic relief of menopause, it is also known for its anti-fatigue effects, skin rejuvenation, and anti-aging functions.
Treatment flow
In consultation with our physicians, the placenta therapy will be given via intramuscular or subcutaneous injection as indicated.
Side Effects
While placenta therapy has a high safety profile, pain or swelling at the injection site, hypersensitivity (rash, fever, pruritus, etc.), headache, a rise in liver function tests (AST, ALT) have been reported. A rare but clinically significant adverse reaction of shock is possible due to its protein and amino acid content derived from human tissue.
Contraindications to treatment
- Women who are pregnant
Important note
To date, there have been no reports of infectious diseases transmitted in Japan or overseas due to the administration of pharmaceuticals made from human placenta, including Laennec. However, the risk of transmission of variant Creutzfeldt-Jakob disease (vCJD) cannot be completely ruled out. For this reason, those who use Laennec will not be able to donate blood through the Japanese Red Cross Society.
* Since its launch in 1974, there have been no reports of infectious disease transmission including viral hepatitis, AIDS, vCJD, etc. caused by the administration of Laennec.