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萝莉社 JAX Paraesophageal Hernia Outcomes Data Bank

  • Status
    Accepting Candidates
  • Age
    18 Years - N/A
  • Sexes
    All
  • Healthy Volunteers
I'm interested
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Description

This is a longitudinal cohort study to better understand the specific factors that are associated with surgical outcome measures as well as Quality of Life following Hiatal/ Paraesophageal hernia surgery. It will contain data extracted from the Electronic Health Record. The goal is to improve the understanding of the factors that affect outcome and quality of life in patients undergoing this procedure.

Details

Protocol number 202400569

Eligibility

Inclusion:

  • Age 18 years or older
  • Work up for a Hiatal/ Paraesophageal hernia repair at 萝莉社 Jacksonville by a surgeon in the division of general surgery
  • Speaks english or spanish

Exclusion:

  • Under 18 years old
  • Emergency Hiatal/ Paraesophageal repair
  • Vulnerable populations (i.e incarcerated)
  • Unwilling or unable to provide consent

Participate in a study

Here are some general steps to consider when participating in a research study:

  1. Step
    1

    Contact the research team

    Call or email the research team listed within the specific clinical trial or study to let them know that you're interested. A member of the research team, such as the researcher or study coordinator, will be available to tell you more about the study and to answer any questions or concerns you may have.

    Primary contact

  2. Step
    2

    Get screened to confirm eligibility

    You may be asked to take part in prescreening to make sure you are eligible for a study. The prescreening process ensures it is safe for you to participate. During the prescreening process, you will be asked some questions and you may also be asked to schedule tests or procedures to confirm your eligibility.

  3. Step
    3

    Provide your consent to participate

    If you are eligible and want to join the clinical trial or study, a member of the research team will ask for your consent to participate. To give consent, you will be asked to read and sign a consent form for the study. This consent form explains the study's purpose, procedures, risks, benefits and provides other important information, such as the study team's contact information.

  4. Step
    4

    Participate

    If you decide to participate in a clinical trial or study, the research team will keep you informed of the study requirements and what you will need to do to throughout the study. For some trials or studies, your health care provider may work with the research team to ensure there are no conflicts with other medications or treatments.