Influence of IQPAS-119 on Post-Marathon Susceptibility to Infections and Others

InQpharm

Status

Completed

Conditions

Upper Respiratory Tract Symptoms

Treatments

Dietary Supplement: IQP-AS-119

Dietary Supplement: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT02873910

INQ/009716

Details and patient eligibility

About

The purpose of this study is to evaluate the benefit and tolerability of IQP-AS-119 for reduction of susceptibility to infections and other complaints after extreme physical stress (participation in a marathon).

Enrollment

75 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Caucasian males and females, 18-65 years of age, residents of Berlin or Brandenburg
Body mass index (BMI) 18.5-26.0 kg/m2
Registered as runner for the 43rd BMW Berlin Marathon 2016
History of at least 2 successful finished marathons (personal record of 3-5.5h within the last 5 years)
History of post-exercise susceptibility to infections (e.g. upper respiratory tract symptoms) and/or other health conditions (infections, stress complaints) after strenuous exercise (eg. marathon, half-marathon, bicycle races, triathlons, heavy training loads) within the last 5 years (to be distinctly documented at screening)
Readiness to comply with all study procedures, in particular:
- Consumption of the investigational product (IP) during the entire treatment period of the study
- Maintaining the habitual diet, with the exception of consumption of maximal 2 garlic cloves per week
- Adapt pre-marathon training / physical activity to generally accepted proven or individually successful training plan
- Adapt post-marathon training / physical activity to generally accepted proven or individually successful recovery plan
- Filling in diaries and questionnaires
Readiness to ensure generally proven or individually successful optimal food intake and rehydration before, during, and after the marathon.
Non-smoker / smoking cessation of last ≥12 months prior to screening
Regular sleeping pattern (no suspicion of sleep disorder) in the three months prior to screening
Stable concomitant, permitted medication (if any) for at least last 2 weeks prior to screening and during the study
Women of child-bearing potential only:
1. negative pregnancy testing (Beta human chorionic gonadotropin (ß-HCG) in urine) at screening
2. commitment to use reliable contraception methods during the entire study

Participation is based upon written informed consent form (ICF) by the participant following written and oral information by the investigator regarding nature, purpose, consequences and possible risks of the clinical study.

Exclusion criteria

Known sensitivity to any ingredients of the IP
Additional strenuous exercise/activity other than regular occupational load, completing training runs / exercises prior the marathon. Additional strenuous exercise/activity other than regular occupational load and recovery exercise loads after the marathon
History of severe cardiovascular disease or collapse during a running event (half marathon, marathon etc.) and/or training
Hypertension (systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg)
Any abnormality observed in screening exercise ECG pointing to an increased cardiovascular risk (alternatively: any abnormality in the results of an exercise ECG performed in the last 6 weeks prior to screening pointing to an increased cardiovascular risk)
Any chronic disease affecting the upper respiratory tract and the lungs, eg. asthma bronchial, chronic obstructive pulmonary disease, or ears-nose-throat (ENT) infection
Acute infection of ENT or upper respiratory tract (URT) within the last month prior to screening
Any nasal abnormalities:
1. History of nasal reconstructive surgery
2. Severe nasal septum deviation or other condition that could cause nasal obstruction
3. Presence of nasal ulcers or nasal polyps
Active organ or systemic diseases including severe cardiovascular disease, diabetes mellitus, renal or liver disorder
Known congenital or acquired immunodeficiency disease (e.g. HIV infection)
Known bleeding disorders such as bleeding ulcers, or haemophilia
Vaccination against influenza within 3 months prior to screening; any vaccination planned during the study
Anticoagulants such as warfarin
Systemic analgesics (other than paracetamol up to 2000mg/day or ibuprofen up to max. 800 mg/day, or if medically indicated and prescribed by a physician), antibiotics (unless medically indicated and prescribed by a physician) or decongestant nose drops / spray (except for isotonic sea water, or if medically indicated and prescribed by a physician) during the study
Use of medications or supplements influencing immune function (e.g. antihistamines, systemic corticosteroids, immune-suppressants), and physical performance, as per investigator's judgement, during the study
Use of any doping substance as listed by the "World Anti-Doping Agency" at present or in the past, unless prescribed by a physician under a '"therapeutic use exemption", per investigator's judgement
Any use of food supplements containing vitamins, minerals, or trace elements, as per investigator's judgement, during the study
Alcohol abuse (men: ≥21 units/week, women: ≥14 units/ week; 1 unit equals approximately 250 mL of beer, 100 mL of wine or 35 mL of spirits)
Women of child-bearing potential: pregnant or breastfeeding
Participation in other studies within the last month prior to screening and during study
Any other clinically significant condition which in the investigator's opinion could interfere with the results of the study or the safety of the subject