Clinical Research

At CLS Health, we are striving to bring new and advanced treatment opportunities to our patients.

For more than 12 years the physicians of CLS Health have partnered with over 100 clinical trials to aid in the development or new treatment options for our patients. Study visits are conducted within the comfort of our practice office(s) with our partner Tranquil Clinical Research. Together, our Clinical Research Trials are research studies designed to test the safety and effectiveness of new medications and treatments.

 

Currently Enrolling Studies

Over Active Bladder Study

Diagnosed with OAB? Participate in a clinical study for a new wearable OAB device

Qualifications: 

  • Be 18 or older
  • Diagnosed with Overactive Bladder
  • Have an average of 10 urinary frequency events per day
  • Have daily access to WIFI

Requires:

  • Wearing an investigational device for 30 minutes 1 to 3 times per week in your home
  • 12-week study period

Contact Us NOW Space is Limited:

  • Tranquility Research
  • Call 713-907-6054
  • There will be compensation for your time

Click here for more information regarding this study or call 713-907-6054

Over Active Bladder Clinical Study Information

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Infant Research Study

Have you been switching your baby’s formula often? Before switching again, please consider the following:

Dr. Palmer at Clear Lake Pediatrics is looking for fussy babies to participate in a 1 month investigational formula research study.

Qualifications: 

  • Full-term, healthy newborns who are 7-42 days of age
  • Babies who being exclusively formula-fed

Participation Includes:

  • Study visits at no cost to you
  • Study formula provided at no cost
  • Compensation for your time will be provided

Contact Us NOW Space is Limited:

  • Tranquility Research
  • Call 713-907-6054
  • There will be compensation for your time

Click here for more information regarding this study or call 713-907-6054

Infant Research Study Information

How to Participate

Participants undergo careful pre-screening and screening steps before they are enrolled in a study. Screening for criteria like age, previous treatments, and other medical conditions are among the screening criteria used to protect a participant’s safety and to ensure researchers obtain the information they need.

Eligible participants meet with one of our trained research coordinator staff to review the study and answer all questions. A document called an informed consent that has been approved by an independent review board (IRB) is reviewed and signed prior to any data collection or testing for the study.

In most cases, participation in a clinical trial incurs no cost to the patient. Sponsors may also offer compensation for time and travel. This information will be discussed during the informed consent review.

Study participation is voluntary. Participants have the right to withdraw from study participation at any time. The decision to withdraw will not result in any penalty nor adversely affect your relationship with your study doctor or practitioner.

 

Study Links

Over Active Bladder

Click here for more information regarding this study or call 713-907-6054

AMHOAB_Advert_12Apr2021

 

Infant Research Study

Click here for more information regarding this study or call 713-907-6054

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