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Postmenopausal Osteoporosis Clinical Research Study

Postmenopausal Osteoporosis Clinical Research Study

Postmenopausal Osteoporosis Clinical Research Study in Las Vegas

If you are over the age of 60 and suffer from Osteoporosis, there is a clinical research study happening now in Vegas that can help treat your condition. Now is your opportunity to explore new treatment options beyond what your doctor is able to offer you; treatment options that are on the cutting-edge of science and research. FDA approved, you can also earn money by taking part in this study. Keep reading to learn more about the Postmenopausal Osteoporosis Clinical Research Study in Las Vegas.

What is Postmenopausal Osteoporosis?

According to the National Library of Medicine, Osteoporosis is a metabolic bone disorder that is characterized by low bone mass and micro-architectural deterioration of bone tissue. Postmenopausal osteoporosis, resulting from estrogen deficiency, is the most common type of osteoporosis. Estrogen deficiency results in an increase in bone turnover owing to effects on all types of bone cells. The imbalance in bone formation and resorption has effects on trabecular bone (loss of connectivity) and cortical bone (cortical thinning and porosity). Fractures of the proximal femur, the vertebrae, and the distal radius are the most frequent osteoporotic fractures, although most fractures in the elderly are probably at least partly related to bone fragility.

Are Clinical Research Studies Safe?

Also according to the US National Library of Medicine, many safeguards are put in place to protect participants. These include:

  • Informed consent is a process used by researchers to provide potential and enrolled participants with information about a clinical study. This information helps people decide whether they want to enroll or continue to participate in the study. The informed consent process is intended to protect participants and should provide enough information for a person to understand the risks of, potential benefits of, and alternatives to the study.
  • In addition to the informed consent document, the process may involve recruitment materials, verbal instructions, question-and-answer sessions, and activities to measure participant understanding.
  • Participants may withdraw from a study at any time, even if the study is not over.

All of Excel Clinical’s studies are HIPAA-compliant, meet all industry safety guidelines, and are governed & monitored by a central ethics committee.

Other benefits you can look forward to as part of the Postmenopausal Osteoporosis Clinical Research Study include:

  • Complimentary consultation and health exam
  • Complimentary lab reports
  • Complimentary study-related medicines
  • Full confidentiality
  • Guaranteed compensation of $1,600

Who Conducts the Postmenopausal Osteoporosis Clinical Research Study?

Vegas Study Clinical Research has extensive experience conducting Phase II through IV clinical trials with many leading pharmaceutical companies. The facility is led and operated by qualified investigators. Every member of the team offers a wealth of experience, a caring personality, and a commitment to ably serving the pharmaceutical industry, the community, and its patients. Our team of clinical research investigators brings knowledge and multiple years of research experience. They also speak English and Spanish.

To learn more about us or to participate in the Postmenopausal Osteoporosis Clinical Research Study, visit us at