Winston Salem, NCNCT04734106Now EnrollingIRB Ready

Interstitial Cystitis Clinical Trial in Winston Salem, NC

Access cutting-edge interstitial cystitis treatment through this clinical trial at a research site in Winston Salem. Study-provided care at no cost to qualified participants.

Sponsored by Wake Forest University Health Sciences

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Expert Care in Winston Salem

Access interstitial cystitis specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related interstitial cystitis treatment provided free

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Check if you qualify for this interstitial cystitis clinical trial in Winston Salem, NC

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Winston Salem

    Convenient for NC residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Winston Salem site if eligible
  4. 4Begin participation

About This Interstitial Cystitis Study in Winston Salem

The purpose of this study is to assess the safety and efficacy of super-concentrated, freeze-dried aloe vera capsules for treatment of interstitial cystitis.

Sponsor: Wake Forest University Health Sciences

Who Can Participate

Inclusion Criteria

Females or males, aged 18 years or older
Females of childbearing potential must agree to use acceptable methods of birth control. Acceptable methods are oral and injectable preparations, double barrier, vasectomized partner, or abstinence.
Participant must sign and date the informed consent.
Participant must report a urinary frequency of at least 11 times per 24-hour day, on average over the previous four weeks.
Participant must report a pain/discomfort score of 4 or greater on a 0-9 Likert scale.
These reported urinary symptoms of frequency and pain/discomfort must have been present for at least the previous 24 weeks prior to the first baseline screening visit.
Participants must report in the baseline voiding diary at least one voided volume greater than or equal to 75cc in a 24-hour period.

Exclusion Criteria

Known allergy or intolerance to aloe vera in any form as reported by the participant or derived from medical records.
History of Bladder tumors (malignant or benign).
Current active bladder or urethral calculus.
History of urethral cancer within the previous five years.
Any disease which, in the opinion of the investigator, may be unstable or have bearing on the outcome of the study, including severe debilitating concurrent medical conditions such as coronary artery disease, azotemia, moderate to severe hepatic insufficiency, etc.
Previous treatment with Cytoxan (cyclophosphamide).
History of cyclophosphamide or chemical cystitis or tuberculosis or radiation cystitis.
History of pelvic radiation treatment, bladder cancer or cancer in situ, or urethral cancer.
History of any other neoplastic process currently requiring systemic, nonprophylactic treatment.
History of urethral diverticulum.
Inability to void spontaneously.
Subjects with interstitial cystitis symptoms alleviated by current therapy regimen.
Uncontrolled diabetes mellitus.
Previous enrollment in an aloe vera study.
Previous use of Desert Harvest super-concentrated, freeze-dried aloe vera capsules.
Any imminent change in residence that could compromise compliance.
Unlikely to be compliant due to unmanaged medical or psychological problem, including dementia, aphasia, or other deficits of cognition or speech/language function that will interfere with the participant's ability to complete the study.
Substance abuse or dependency problem within the past two years for which patient received no treatment. Male-Specific Exclusion Criteria:
Males with a history of prostate cancer within the previous five years.
Males with a prostatic infection within the previous three months. Female-Specific Exclusion Criteria:
Females with a history of uterine, cervical, or vaginal cancer within the previous five years.
Pregnant or lactating females.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Winston Salem?

Yes, this clinical trial (NCT04734106) has an active research site in Winston Salem, NC that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Interstitial Cystitis Treatment Options in Winston Salem, NC

If you're searching for interstitial cystitis treatment options in Winston Salem, NC, this clinical trial (NCT04734106) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Winston Salem research site is actively enrolling participants for this clinical trial. You'll receive care from experienced interstitial cystitis specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all interstitial cystitis clinical trials near you to find additional studies recruiting in your area.

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