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Study No Longer Active

Introducing the Nirvana Clinical Sleep Study

Menopause induced sleep disturbances might interrupt your peaceful nights. Are you finding menopause is waking you up at night, and you’ve also had a hysterectomy? Then read on and get more information on the NIRVANA clinical sleep study.

About the Nirvana Clinical Sleep Study

The Nirvana Clinical Sleep Studies objective is to determine whether an investigational medication may improve sleep disturbances associated with menopause.

You may be able to join the Nirvana Sleep  study if you:

  • Must have had a Hysterectomy 6 weeks or more ago
  • Currently experiencing hot flashes
  • Must be age 40-65
  • Receive compensation of up to $1000 for inconvenience and travel

Other criteria will be checked at the first visit and will need to be met to confirm your eligibility for this study.

Menopause disturbing your sleep?

Consider joining the NIRVANA study – a clinical study being conducted to find out if an investigational medication improves sleep disturbances associated with menopause.

Complete The Questionnaire Below To Submit Your Information For Future Studies

Study Overview

Description:

The objective of this study is to determine whether an investigational medication may improve sleep disturbances associated with menopause.

There are 3 study periods. The screening period lasts 4–6 weeks and consists of 3 study center visits. The second visit during screening will be a 2-consecutive night stay at a sleep center. The study treatment period lasts 12 weeks. The 12-week study treatment program includes two more (2-night) stays at a sleep center and one telephone visit. Approximately 4 weeks after you stop taking the study drug, there is one follow-up visit that is conducted by telephone.

About Clinical Studies

A research study involving human subjects is designed to answer specific questions about the safety and/or efficacy of an intervention (drug, treatment, device, or other products), or new ways of using a known drug, treatment, device, or product before or during an investigational drug or product is made available to the public.

  • Clinical studies follow specific rules and regulations to protect the rights, safety, well-being, and confidentiality of study participants. Clinical studies must be approved by an independent ethics committee before it can begin.
  • The results help competent regulatory authorities to decide if a drug is safe and/or efficacious

Your participation in the Nirvana Sleep clinical research study is completely voluntary and can be stopped at any time and for any reason. If you decide not to participate, it will not affect your medical care now or in the future.