Status:
COMPLETED
Safety and Efficacy of Cunermuspir on Energy, Strength, and Fatigue in Patients With Nerve or Muscle Pain
Lead Sponsor:
Mitosynergy LLC
Conditions:
Neuralgia
Myalgia
Eligibility:
All Genders
18-75 years
Phase:
PHASE1
PHASE2
Brief Summary
Male and female participants were selected based on chronic neuromuscular pain. Patients were instructed to take two doses of the placebo or cuprous nicotinic acid chelate Cunermusmir twice a day for ...
Detailed Description
A total of 72 subjects were consented and screened, with 56 subjects (28 males and 28 female) being eligible to participate in the study. Fifty-six subjects with muscle/nerve pain were randomized at a...
Eligibility Criteria
Inclusion
- Male or female age 18-75
- If female, subject is not of child bearing potential. Defined as females who have
- had a hysterectomy or oophorectomy.
- bilateral tubal ligation or are post-menopausal (natural or surgically with \> 1 year since last menstruation).
- Female subject of childbearing potential must agree to use a medically approved method of birth control and have a negative urine pregnancy test result. Acceptable methods of birth control include: Hormonal contraceptives including oral contraceptives, hormone birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing), injectable contraceptives (Depo--Provera, Lunelle), or hormone implant (Norplant System), Intrauterine devices, Vasectomy of partner, Total Abstinence
- Subject has unresolved persistent muscle or nerve pain (muscle or nerve pain population)
- Subjects using other therapies for nerve/muscle pain (e.g., exercise, TENS, acupuncture, exercise, psychotherapy, massage, physiotherapy, etc), must be used at a stable schedule for 1 month prior to the trial and subject agrees to continue these therapies at the same schedule during the trial avoiding changes in frequency or intensity and to record therapies in the study diary
- Agrees to comply with study procedures
- Has given voluntary, written, informed consent to participate in
- the study
Exclusion
- Women who are pregnant, breastfeeding, or planning to become pregnant during the course of the trial
- Planned surgery during the course of the trial
- Use of prescription drugs for fibromyalgia or nerve pain (e.g.Lyrica, Cymbalta and Savella and others).
- Use of prescription medications for depression, anxiety or other mental disorders
- Requires the use of prescription drugs to control pain (other than provided rescue medication)
- Use of oral or topical prescription or over the counter medications or natural health products for pain relief 3 days prior to randomization and during the trial (other than provided rescue medication)
- Use of natural health products including vitamins and minerals within 3 days prior to randomization and during the trial
- Use of blood thinning medications (e.g. warfarin)
- Chronic lyme disease or chronic parasitic infections
- Uncontrolled hypertension defined as untreated systolic blood pressure \> 160 mmHg and/or diastolic blood pressure \> 100 mmHg
- Subjects with diabetes
- History of bleeding disorders, or significant blood loss in the past 3 months
- Alcohol use \>2 standard alcoholic drinks per day and/or alcohol or drug abuse within the past year
- Allergy or sensitivity to study supplement ingredients or acetaminophen
- Participation in a clinical research trial within 30 days prior to randomization
- Individuals who are cognitively impaired and/or who are unable to give informed consent
- Any other condition which in the Investigator's opinion may adversely affect the subject's ability to complete the study or its measures or which may pose significant risk to the subject
Key Trial Info
Start Date :
January 28 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 29 2014
Estimated Enrollment :
56 Patients enrolled
Trial Details
Trial ID
NCT04737278
Start Date
January 28 2014
End Date
September 29 2014
Last Update
April 20 2021
Active Locations (1)
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1
KGK Synergize now KGK Science
London, Ontario, Canada, N6A 5R8