Shopping CartPulmonary Fibrosis PageUterine Fibroid PagePeyronies PageBuy Serracor-NK
 
 
 
Serracor, Serracor NK, Uterine Fibroids, Uterine Fibroid, Fibroid Treatment, Pulmonary Fibrosis, Peyronies DiseaseSerracor, Serracor NK, Serracor-NK, Fibroid Treatment, Uterine Fibroids, Uterine Fibroid, Pulmonary Fibrosis TreatmentUterine Fibroids, Uterine Fibroid, Fibroid Treatment, Pulmonary Fibrosis, Peyronies Disease, Serracor, Serracor NK Pulmonary Fibrosis Treatment, Uterine Fibroids, Uterine Fibroid, Uterine Fibroid Treatment, Serracor, Serracor-NKSerracor, Serracor NK, Uterine Fibroids, Uterine Fibroid, Peyronies, Pulmonary FibrosisSerracor, Serracor NK, Uterine Fibroids, Uterine Fibroid, Pulmonary Fibrosis, Fibroids, Peyronies diseaseSerracor, Serracor NK, Uterine Fibroids, Uterine Fibroid, Pulmonary Fibrosis Treatment, Peyronies Disease TreatmentSerracor NK, Serracor, serrapeptase, uterine fibroid treatment, uterine fibroids, uterine fibroid, pulmonary fibrosis, peyronies treatment
 
 
Serracor-Nk Clinical Studies 
Serracor-NK Clinical Information 

Research and Clinical Studies done on the main ingredients in Serracor-NK

The research behind Enzyme Therapy for Black Lung Disease?

Serrapeptase has been in use since 1979. Since then the effacous anti-inflammatory response with the use of Serrapeptase has been shown not only as new way to eliminate fibrin or fibrous formations in the body systemically but is showing promising results for Chronic inflammation in the lungs along with the dispelling of mucus in the lining of the arterial walls in the lungs. Studies have shown the positive effects of Serrrapeptase for the use of Pulmonary Fibrosis.

Serrapeptase Study #1

 Effect of the proteolytic enzyme serrapeptase in patients with chronic airway disease.  

OBJECTIVES: The proteolytic enzyme serrapeptase (SER) is widely used in clinical practice in Japan. We investigated the effect of SER on sputum properties and symptoms in patients with chronic airway diseases. METHODS: This study was an open-labelled trial with a non-treatment control group. Patients were randomly assigned to oral treatment with (n = 15) and without (n = 14) SER 30 mg/day for 4 weeks. Patients collected sputum samples for about 4 h in the morning on the day the trial began and 4 weeks later. We measured the amount of sputum by weighing. Part of each sputum sample was weighed and then completely dried and reweighed. The percentage solid component, viscosity and elasticity of the sputum were measured. Mucociliary transportability index was measured using ciliated bovine trachea ex vivo. Sputum smears were also prepared to count sputum neutrophils. Patients' symptoms were assessed by a questionnaire that used a visual analogue scale. RESULTS: After 4 weeks of SER treatment, sputum weight in the morning, percentage solid component, viscosity and elasticity of sputum, sputum neutrophil count, frequency of coughing and frequency of expectoration significantly decreased. The mean mucociliary transportability index increased from 13.3 +/- 1.8 to 24.4 +/- 2.5 (P = 0.0103). CONCLUSIONS: SER may exert a beneficial effect on mucus clearance by reducing neutrophil numbers and altering the viscoelasticity of sputum in patients with chronic airway diseases.3

Serrapeptase Study #2

Evaluation of Serratia peptidase in acute or chronic inflammation of otorhinolaryngology pathology: a multicentre, double-blind, randomized trial versus placebo.

The efficacy and tolerability of Serratia peptidase were evaluated in a multicentre, double-blind, placebo-controlled study of 193 subjects suffering from acute or chronic ear, nose or throat disorders. Treatment lasted 7-8 days, with the drug or placebo being administered at a rate of two tablets three times a day. After 3-4 days' treatment, significant symptom regression was observed in peptidase-treated patients. There was also a significant reduction in symptoms after 7-8 days for patients in both treatment groups but the response was more marked in those patients receiving the active drug. Statistical comparison between the two groups confirmed the greater efficacy and rapid action of the peptidase against all the symptoms examined at both stages. Tolerance was found to be very good and similar for both groups. It is concluded that Serratia peptidase has anti-inflammatory, anti-oedemic and fibrinolytic activity and acts rapidly on localized inflammation.4

Another effacious systemic enzyme Nattokinase  has been used by Japanese Pharmaceutical companies for anti-thrombosus and blood anti-coagulation. Nattokinase like Serrapeptase has had a good amount of clinical studies behind it, to prove not only is Nattokinase effective for thinning the blood and reversing the formation of blood clots but it has shown to be one of the strongest fibrinolytic activity systemically in the blood stream.

The use of Nattokinase for Black Lung Disease

Another effacious systemic enzyme Nattokinase  has been used by Japanese Pharmaceutical companies for anti-thrombosus and blood anti-coagulation. Nattokinase like Serrapeptase has had a good amount of clinical studies behind it, to prove not only is Nattokinase effective for thinning the blood and reversing the formation of blood clots but it has shown to be one of the strongest fibrinolytic activity systemically in the blood stream.

Nattokinase Study #1

Nattokinase decreases plasma levels of fibrinogen, factor VII, and factor VIII in human subjects

Nattokinase, a serine proteinase from Bacillus subtilis, is considered to be one of the most active functional ingredients found in natto. In this study, we hypothesized that nattokinase could reduce certain factors of blood clotting and lipids that are associated with an increase risk for cardiovascular disease (CVD). Thus, an open-label, self-controlled clinical trial was conducted on subjects of the following groups: healthy volunteers (Healthy Group), patients with cardiovascular risk factors (Cardiovascular Group), and patients undergoing dialysis (Dialysis Group). All subjects ingested 2 capsules of nattokinase (2000 fibrinolysis units per capsule) daily orally for 2 months. The laboratory measurements were performed on the screening visit and, subsequently, regularly after the initiation of the study. The intent-to-treat analysis was performed on all 45 enrolled subjects. By use of mixed model analysis, a significant time effect, but not group effect, was observed in the change from baseline of fibrinogen (P = .003), factor VII (P < .001), and factor VIII (P < .001), suggesting that the plasma levels of the 3 coagulation factors continuously declined during intake; also, the extents of decrease were similar between groups. After 2 months of administration, fibrinogen, factor VII, and factor VIII decreased 9%, 14%, and 17%, respectively, for the Healthy Group; 7%, 13%, and 19%, respectively, for the Cardiovascular Group; and 10%, 7%, and 19%, respectively, for the Dialysis Group, whereas blood lipids were unaffected by nattokinase. No significant changes of uric acid or notable adverse events were observed in any of the subjects. In summary, this study showed that oral administration of nattokinase could be considered as a CVD nutraceutical by decreasing plasma levels of fibrinogen, factor VII, and factor VIII.5

 

Nattokinase Study #2

 

Enhancement of the fibrinolytic activity in plasma by oral administration of nattokinase.

 

The existence of a potent fibrinolytic enzyme (nattokinase, NK) in the traditional fermented food called 'natto', was reported by us previously. It was confirmed that oral administration of NK (or natto) produced a mild and frequent enhancement of the fibrinolytic activity in the plasma, as indicated by the fibrinolytic parameters, and the production of tissue plasminogen activator. NK capsules were also administered orally to dogs with experimentally induced thrombosis, and lysis of the thrombi was observed by angiography. The results obtained suggest that NK represents a possible drug for use not only in the treatment of embolism but also in the prevention of the disease, since NK has a proven safety and can be mass produced.6

Toll Free USA 1-877-404-8804 / INT'L 1-602-404-3384

Pivotal Health Products Corp.
4727 E. Bell Road, Suite 45-447

Phoenix, AZ  85032-9339

Toll Free in USA 1-877-404-8804
International calls only 1-602-404-3384
Email: sales@pivotalhealth.info


Do not take Serracor-NK if your are currently taking blood thinning medication.  Serracor-NK is not recommended for women who are pregnant or nursing as these groups have not been clinically tested.  As always, consult with your doctor before taking Serracor-NK.

*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease. For all conditions or illnesses, see a healthcare professional for a full evaluation, diagnosis or treatment plan.