Last updated: March 26, 2024
Sponsor: Super Inspired LLC
Overall Status: Active - Recruiting
Phase
N/A
Condition
N/ATreatment
Supplementation with Nirvana Super Pro Liquid Supplements
Non-Supplementation Group
Clinical Study ID
NCT06203691
11495
Ages 45-80 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Male and female subjects will be enrolled into the study.
- Age ≥45-80 years.
- Free of liver and kidney diseases, and with no evidence of uncontrolled hypertension.
- Does not have a chronic disease that affects calcium or bone metabolism (i.e., asthmawith chronic use of high dose steroids, inflammatory bowel disease, Crohn's disease,primary hyperparathyroidism, seizure disorder with use of phenobarbital, etc.).
- Not classified as morbidly obese (body mass index (BMI) >43 kg/m2).
- Six weeks since major surgery (three weeks since minor surgery).
- Total joint replacement is not a revision of previous joint replacement.
- Willing to consume dietary supplements for the study period.
- Individuals diagnosed with osteoporosis, or a bone density >2.0 standard deviationsbelow the mean, will not be enrolled in the study.
- No other serious medical illness.
- Physicians have placed no restriction on physical exercise.
- Patient is scheduled for a total knee or hip replacement and agrees to consume the 28-day pre-operative regime.
Exclusion
Exclusion Criteria:
- Evidence of liver and kidney diseases, uncontrolled hypertension, or Type I or IIdiabetes mellitus requiring insulin for glucose control.
- The presence of a chronic disease that affects calcium or bone metabolism (i.e.,asthma with chronic use of high dose steroids, inflammatory bowel disease, Crohn'sdisease, primary hyperparathyroidism, seizure disorder with use of phenobarbital,etc.).
- Classified as morbidly obese (body mass index (BMI) >43 kg/m2).
- Less than six weeks since major surgery or three weeks since minor surgery.
- Surgery is a revision of a previous total joint replacement.
- Not willing to consume nutritional supplements for the study period.
- Individuals diagnosed with osteoporosis, or a bone density >2.0 standard deviationsbelow the mean, will not be enrolled in the study.
- Other serious medical illness, which the subject's doctor or medical review team hasdecided affects the subject's ability to participate in the study. For example,pathological hip fracture or cancer disease in active phase or undergoing treatment (radiotherapy or chemotherapy).
- History of blood clots and/or the use of blood thinning medications
- Subjects on high dose vitamin D therapies (i.e., 50,000 IU vitamin D).
Study Design
Total Participants: 100
Treatment Group(s): 2
Primary Treatment: Supplementation with Nirvana Super Pro Liquid Supplements
Phase:
Study Start date:
February 21, 2024
Estimated Completion Date:
August 30, 2024
Study Description
Connect with a study center
University Orthopedics Center
Altoona, Pennsylvania 16602
United StatesActive - Recruiting
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