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Troubled By Frequent Nighttime Urination?

Explore Nighttime Urinary Incontinence Management Clinical Trials in Michigan!

Nighttime urination, also known as nocturia, can significantly disturb your sleep and affect your overall quality of life. Frequent waking up to urinate leads to sleep fragmentation, which can result in sleep deprivation, fatigue, irritability, and reduced cognitive function during the day. If you find yourself waking up two to three times or more during the night to urinate, it may indicate a need for further evaluation and treatment.

Revive Research Institute is conducting Nocturnal Enuresis Clinical Trials in Michigan to evaluate the safety and efficacy of female urinary incontinence device to help manage nighttime urinary symptoms.

You may qualify for the Nocturia Clinical Research Trial near you if you are:

  • Female ≥ 18 years of age
  • Using diapers or equivalent at night for urine output management

*Additional criteria may apply

*Take part in paid Nocturia Clinical Research Trial at no cost to you or your medical insurance. You will be reimbursed financially for your time and travel. In addition, all participants receive study-related care from an experienced research team.
*If you are interested in participating in the Nocturnal Enuresis Clinical Trials in Dearborn, Michigan or would like more information, please fill out the form so we can determine if you qualify for the study and contact you. Note that this is an entirely voluntary decision.

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About Nocturnal Enuresis Clinical Research Trials in Michigan

Frequent nighttime urination can be caused by various factors, including aging, hormonal changes, increased fluid intake before bed, or underlying medical conditions such as diabetes, bladder disorders, or sleep apnea. It is estimated that in the US approximately 50 million people suffer from this condition. We are conducting clinical trials for potential treatment of Nocturia for females (≥ 18 years) with frequent nighttime urination to assess the safety and efficacy of female urinary incontinence device.

Nocturia Clinical Research Trials will be conducted in several locations across the United States, including Michigan. To ensure study eligibility, all participants must comply with study procedures. Eligible participants will be randomized into two groups to evaluate safety and efficacy of female urinary incontinence device. These devices will be used each night for 4 weeks to assess their effectiveness in reducing sleep disturbances due to frequent urination.

*There is no cost to you, your private medical insurance, or the public health insurance plan for study procedures. The study-related procedures, and visits will be provided at no charge throughout the duration of the study.

Get Started: What to Expect?

Is frequent nighttime urination affecting your sleep? If you are suffering from frequent nighttime urination and want to participate in a paid Nocturia Clinical Research Trials, please reach out to us by filling in the form above. One of our study team representatives will contact you to see if you are eligible for this study (pre-screening).

Someone from the research team will ask you to sign an Informed Consent Form (ICF) if you meet the study criteria during the pre-screening process. Once you sign up for the ICF, we will invite you for a screening visit to our clinical site; this will be an initial visit. After that, you will undergo a series of health-related questions and tests to confirm your eligibility as a participant.

Once you receive confirmation of eligibility, you will formally be a part of the Nocturia Clinical Research Trials. You will receive all the information about the research study you might enroll in during the ICF process. We encourage you to ask as many questions as you would like before deciding to participate.

*All study-related care is provided free of cost. Complete physical examination and other study-related assessments will be done by expert physicians and health care experts.

Length of study

Approx. 4 weeks

Number of study visits

Approx. 7 visits

Location

Michigan

About Nocturia & It’s Symptoms

Nocturnal Enuresis Clinical Trials

Nocturia is the medical term for waking up multiple times during the night to urinate. While occasional nighttime trips to the bathroom may not be concerning, frequent urination at night can be disruptive and signal an underlying issue. Nocturia is often considered one of the most bothersome urinary symptoms, affecting women, particularly as they age.

This condition can significantly impact the quality of sleep, leading to insomnia, daytime fatigue, and reduced overall well-being. The disruption to normal sleep patterns can also cause irritability, difficulty concentrating, and mood swings.

Vasomotor or Menopause Symptoms

  • Waking up multiple times during the night to urinate
  • A persistent urge to urinate
  • Experiencing reduced bladder control
  • Increased fatigue and drowsiness during the day

Frequently Asked Questions (FAQs)

How many times do you wake up to urinate for it to be considered nocturia?

Nocturia is typically diagnosed when you wake up two or more times a night to urinate.

Can nocturia be treated?

Yes, nocturia can often be managed or treated through lifestyle changes, medications, or addressing the underlying causes.

Is frequent nighttime urination a sign of a serious condition?

While it can be caused by less serious factors, nocturia can also be a symptom of an underlying condition like diabetes or an enlarged prostate. It’s essential to consult a healthcare professional for proper evaluation.

Will my medical information be kept private?

Yes, your personal health information will be handled in a private manner by the research doctor and study staff. All your personal and health-related information will be kept confidential under the privacy rule of HIPAA (Health Insurance Portability and Accountability Act).

Do I have to pay to be a part of the Nocturnal Enuresis Clinical Trials near me?

Participation in the Nocturnal Enuresis Clinical Trials in Michigan is free of cost to you and your health insurance. If you qualify and decide to participate, you will be compensated for your time and travel. Details of the stipend will be given to you once you complete the screening process and move on to the informed consent process.

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Revive Research Institute, Inc.

28270 Franklin Road
Southfield, MI
48034

T: 248-564-1485
E: info@rev-research.com