AzTrials
AzTrials

AcidosisNCT01831492

Effects of Zeolite + Dolomite on Performance and Acidosis

A study testing zeolite + dolomite and cellulose in people with Acidosis and Oxidative Stress, run by Green Beat at 1 site in Austria.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Purpose: This study investigates the effects of dietary zeolite + dolomite on performance, exercise-induced acidosis, oxidative stress, inflammation and intestinal barrier dysfunction in trained people. Read more about this study

Who is it for?
Ages 20 to 50 yearsHealthy volunteers can take part
Conditions the study is for
Acidosis, Oxidative Stress, Inflammation
What is being tested?
zeolite + dolomite and cellulose
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
56 participants
Where
1 siteAustria
Study dates
Apr 2013to Dec 2014
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 50 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • trained people
  • non-smokers
  • body fat: 20-30%
  • 4wk wash-out 20-50 years old

Who cannot join

  • sedentary people
  • smokers
  • people not eligible for exercise
  • high/low body fat
  • people taking supplements
  • to young/old people

Trial locations and contacts

1 site in 1 country.

Austria1 site
  • Green Beat

    Graz, 8042

Other trials in Austria

About this study

Official title: Effects of Dietary Zeolite + Dolomite on Performance, Exercise-induced Acidosis, Oxidative Stress, Inflammation and Intestinal Barrier Dysfunction in Trained People

Purpose:

This study investigates the effects of dietary zeolite + dolomite on performance, exercise-induced acidosis, oxidative stress, inflammation and intestinal barrier dysfunction in trained people.

Hypotheses (H1):

Zeolite + dolomite increase performance in an ergometer step test Zeolite + dolomite reduce exercise-induced acidosis Zeolite + dolomite reduce oxidative stress Zeolite + dolomite reduce inflammation Zeolite + dolomite improve intestinal barrier dysfunction

Read the detailed description

The application of adequate nutraceuticals for sporty people´s performance and health becomes more and more interesting for athletes and their carers. There are also great opportunities for product providers in this field to act commercially profitable.

Beside the main goal - to achieve improved performance - modern sport nutraceuticals should support immunity of athletes in all corners of health. One of the most interesting approaches in this field is to promote performance and health via dietary zeolites. Zeolites are synthetic microporous crystals containing AIO4 and SiO4 tetrahedrons. It is hypothesized that in human body these silicates act as gut-located adsorbents of chymus molecules or as ion-exchangers, catalysts, detergent builders or antidiarrheic agents (1, 2, 3, 4). These - mainly physical - effects of dietary used zeolite might also influence the chief issues of modern sport nutrition: performance, acidosis, oxidative stress, inflammation, gastrointestinal complaints and associated impacts on immunity and health.

The investigators hypothesize that the physical effects of zeolite affect the metabolism in the gut and exert systemic physiological/biochemical benefits in regard to human´s exercise performance, redox biology, inflammatory processes, acid-base balance, and even intestinal barrier integrity/function. All these postulated benefits would have tremendous impact on sports performance. However, up to date no clinical study is reported on PubMed that addresses these chief aims of sport nutrition in the context of zeolite supplementation.

GOALS

This protocol describes a study that investigates the effects of dietary zeolite + dolomite (Product name: "PANACEO SPORT") on performance, exercise-induced (acute or chronically) acidosis, oxidative stress, inflammation and intestinal barrier dysfunction. This is a randomized, placebo-controlled, double-blinded, parallel-grouped study design. In detail, the investigators want to assess the effects of dietary zeolite + dolomite (the commercially available product "PANACEO-SPORT") on:

  1. Aerobic performance capability and maximum oxygen uptake (primary outcome)
  2. Lactate kinetics and maximum lactate concentrations in blood (secondary outcome)
  3. Oxidative stress (OS)/redox biology and inflammation (tertiary outcome)
  4. Intestinal barrier integrity and endotoxemia (quaternary outcome) The investigators hypothesize that the intake of the product will beneficially influence outcomes 1-4 (H1-hypotheses 1-4: "Supplementation will influence..."). MERITS of this study Data of this project will provide knowledge regarding the effects of zeolite and dolomite on aerobic performance, lactate kinetics, redox biology, inflammation and integrity of intestinal barrier. Results will help us to identify how to support chronically exercising people to optimize their performance and health. METHODS
  • Subjects: 56 healthy men, non-professional but homogeneously trained (>50ml/kg/min) triathletes and/or cyclists and/or dual athletes, non-smokers, 20-50 yrs, comparable body fat content (<20%) and psycho-physical stress profile, non-medicated, preventive medical check-up and actual proofed eligibility to conduct sports, pre-selection via telephone interviews.
  • Design: randomized, double-blinded, placebo-controlled, 2-arm parallel-group design. One arm is the placebo group, the second arm receives zeolite + dolomite ("PANACEO-SPORT"). After a wash-out of 4wk from any food supplements, also from specific dietetic and drug treatment, a period of 12wk with supplementation or placebo follows. At 0wk, 4wk and 12wk we conduct performance diagnostics. At 0wk and 12wk we collect blood and stool.
  • Treatment: Subjects receive 6 capsules per day of zeolite + dolomite ("PANACEO-SPORT") or placebo capsules with identical appearance. Subjects will be instructed to consume 3 capsules with the first meal of the day and 3 capsules with the last meal of the day. We recommend to dispense one box per subject and to produce 60 boxes containing 600 capsules each (lasting for 100 days in maximum).
  • Surrogate markers/parameters from blood and stool are measured at 0wk and 12wk. Blood samples are collected before the exercise tests. The subjects will bring the samples of their last stool before the exercise tests (at weeks 0 and 12) directly to the exercise physiology laboratory. For blood lactate - in the context of performance diagnostics at weeks 0, 4 and 12 - we collect capillary earlobe blood before, during and until 30 minutes post exercise.
  • Subjects monitor stool appearance via Bristol stool scale/protocol. This is conducted the week before the first exercise test and in the 12th week.
  • Quality of life survey is conducted in the running in period (stress profile)
  • The week before the exercise test it is necessary to adhere to a 4-day diet plan (the last 4 days before the test) and to conduct a 7-day food recording. These sanctions are necessary to match carbohydrate, fat, protein and micronutrient intake and to exclude diet-associated biased lactate kinetics. MARKERS/PARAMETERS
  • Performance diagnostics: maximum performance in watt (Pmax), maximum oxygen uptake capacity (VO2max), CO2 exhalation, CO2/O2 ratio, lactate kinetics, maximum lactate, lactate turnpoint 1 (LTP1), lactate turnpoint 2 (LTP2) and anaerobic threshold (ANS), respiratory quotient, EKG for cardiocirculatory innocuousness.
  • Minerals (serum/plasma) and standard blood chemistry: Mg, Ca, Fe, K, Na, Al, Si, P, Cl, ALT, AST, creatinine, ferritin, transferrin, uric acid, vitamin C, free testosterone, SHBG (testosterone transporter), FAI (= free androgen index = Testosterone x 100/SHBG).
  • OS/redox biology (serum/plasma): carbonyl proteins (CP), F2-isoprostanes, total oxidation status (TOS), proteinogenic antioxidant capacity (PAOC), non-proteinogenic antioxidant capacity (NPAOC), DNA strand breaks, glutathione peroxidase 3.
  • Inflammation/immunity (blood/serum/plasma): TNF-alpha, IL-6, IL-8, IL-10, IL-22.
  • Intestinal barrier integrity and endotoxemia: Zonulin (stool), claudin1 and claudin2 (stool), lipopolysaccharides (blood), toll-like receptors (TLR2 and TLR4 from blood), gut profile "basis" (kind and number of colonies, Calprotectin, α1-antitrypsin etc).
  • Body fat determination and distribution via lipometry (non-invasive) at weeks 0 and 14. BLOOD SAMPLING
  • Week 0: At rest, after 4wk wash-out and before 1st performance diagnostics
  • Week 12: At rest, after 12wk before 3rd performance diagnostics
  • Capillary blood from earlobe to determine lactate is drawn before, during and after exercise at weeks 0, 4 and 12: at each step of exercise and 3, 6, 9, 12, 15, 20 and 30 min post exercise to evaluated recovery lactate kinetics. STOOL SAMPLING
  • Week 0: At rest, after 4 wk wash-out and before 1st performance diagnostics
  • Week 12: At rest, before 3rd performance diagnostics PROTOCOLS/QUESTIONNAIRES
  • Stool protocol is conducted the week before 1st and 3rd performance testing
  • Food habits are documented by food recording and the diet plan the last week prior to each exercise test, at weeks 0, 4 and 12
  • Exercise and trainings habits are evaluated by the sport scientist via interview before each performance testing
  • Psycho-social well-being and stress perception are evaluated with the "Quality of Life-BREF" questionnaire (SF36) before the 1st and 3rd performance testing PERFORMANCE DIAGNOSTIC (PD) PD is a cycle-steptest-ergometry to performance/watt maximum, lactate maximum and VO2max.. After 3 min rest on the cycle ergometer, subjects start exercise with another 3 min warm up at 60 watt. Then they increase exercise intensity by 15 watt per min (with constant 80 rpm) until exhaustion/VO2max. After reaching exhaustion/VO2max, candidates continue to perform at low intensity (at 30% of Pmax) for further 30 minutes to observe recovery lactate kinetics. All tests are supervised by a physician and a sport scientist. Before each test, volunteers are also checked by the physician. PD is conducted at:
  • Week 0: 1st performance diagnostics = last selection of candidates (detailed medical check, standard blood chemistry panel)
  • Week 4: 2nd performance diagnostics
  • Week 12: 3rd and last performance diagnostics LIPOMETRY
  • Week 0: At rest, after 4wk wash-out and before 1st performance diagnostics
  • Week 12: At rest, after 12wk of supplementation and before 3rd performance diagnostics SAMPLE SIZE CALCULATION \& RANDOMIZATION Sample size calculation is based on the expectation of an 8% increase in performance capability (in watt) after 4 weeks of treatment with zeolite + dolomite ("PANACEO-SPORT"), compared to placebo (no change). The investigators expect an average Pmax of 345 watt in this trained cohort, a standard deviation of 10%, and chose a power of 80% for this 2-arm design (1:1 distribution of placebo/verum). This calculation revealed a number of 50 subjects. Drawing into account a drop out rate of 10%, we recommend a sample size of 56 subjects, 28 in each group. Subjects will be randomized into blocks of 4 (2 verum and 2 placebos in each block) and sequentially numbered (www.randomization.com). To guarantee a balanced distribution in performance capability/VO2max between groups (verum vs. placebo) we will conduct stratification via VO2max rank statistics. The allocation of the capsules/boxes will be conducted after the completed 1st exercise test session. Boxes will be delivered by mail and in 2 tranches (a 7 blocks or 28 subjects), separated by a week. This scheme considers a one week period to check 28 subjects and therefore ensures equal duration of treatment for all candidates. STATISTICAL ANALYSES For blood and stool data we will use an univariate, two-factorial analysis of variance (ANOVA). Factors: "treatment" (= placebo vs product) and "time" (= week 0 vs week 12). For lactate and other performance diagnostic parameters we use a three-factorial repeated measures ANOVA with the additional factor "session" (test 1, 2, 3). This statistical test method ensures the consideration of all before-, during- and after- measurements. Further, we will use non-parametric tests, descriptive statistics, and - if indicated - correlation analyses.
Being tested
zeolite + dolomite, cellulose
Keywords
performance, acidosis, oxidative stress, inflammation, oxygen uptake
Medical subject headings
Acidosis, Inflammation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • zeolite + dolomiteDevice

    Also called Panaceo Sport

    Given for 12 weeks, after a 4 weeks wash- out of all supplements/drugs

  • celluloseDevice

    Also called placebo

    given for 14 weeks

Study groups in NCT01831492
Study groupRoleWhat they receive
zeolite + dolomiteActive comparator28 trained subjects receive encapsulated zeolite + dolomite
Receives: Device: zeolite + dolomite
cellulosePlacebo comparator28 trained subjects receive encapsulated micro-crystalline cellulose
Receives: Device: cellulose

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change of aerobic performance capability between baseline, 4 and 12 weeks

    Zeolite and Dolomite might influence maximum aerobic performance due to attenuated lactate accumulation in a step test ergometry

    Measured: 0, 4, 12 weeks

Secondary outcomes (1)
  1. Change of lactate concentrations in blood between baseline, 4 and 12 weeks

    Lactate accumulation and -kinetics is influenced by dietary zeolite and dolomite supplementation

    Measured: 0, 4, 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Apr 2013 (estimated)
  2. Study startApr 2013
  3. Primary completionMay 2014
  4. Study completionDec 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
56 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01831492
Sponsor's protocol ID
25-217 ex 12/13
Other IDs
PSS
Status last verified
Feb 2016
First submitted
9 Apr 2013
Last updated
10 Feb 2016
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A study testing zeolite + dolomite and cellulose in people with Acidosis and Oxidative Stress, run by Green Beat at 1 site in Austria.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Feb 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Austria. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change of aerobic performance capability between baseline, 4 and 12 weeks (time frame: 0, 4, 12 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Feb 2016.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in