Pittsburgh, PANCT03434392Now EnrollingIRB Ready

Chronic Pancreatitis Clinical Trial in Pittsburgh, PA

Access cutting-edge chronic pancreatitis treatment through this clinical trial at a research site in Pittsburgh. Study-provided care at no cost to qualified participants.

Sponsored by Anna Evans Phillips

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Expert Care in Pittsburgh

Access chronic pancreatitis specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related chronic pancreatitis treatment provided free

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Check if you qualify for this chronic pancreatitis clinical trial in Pittsburgh, PA

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Why Participate?

  • No-Cost Study Care

  • Local to Pittsburgh

    Convenient for PA 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 Pittsburgh site if eligible
  4. 4Begin participation

About This Chronic Pancreatitis Study in Pittsburgh

Quantitative Sensory Testing (QST) is a novel investigative technique used in other pain conditions to evaluate patterns of chronic pain, and in this study will be used to elucidate pain patterns in patients with Chronic Pancreatitis (CP). QST uses a specific series of standardized stimulations to map the pain system. QST has the potential to change and improve the treatment paradigm for patients with CP and may eventually be able to predict response to invasive CP therapies.

Sponsor: Anna Evans Phillips

Who Can Participate

Inclusion Criteria

Subjects with no pancreatic disease and no abdominal pain, or patients with a diagnosis of functional dyspepsia.
Subjects are 18 years or older in age
Subjects must be able to read and understand the study information.
Personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
Subject is willing and able to comply with the scheduled visits, questionnaires, treatment plan, and other study procedures.
Suspected CPs Inclusion Criteria
Subjects are 18 years or older in age
Subjects with a) Indeterminate CP (Cambridge 1 or 2 on CT scan or MRI/MRCP) who have abdominal pain without prior history of AP, or b) those with acute (AP) or recurrent acute pancreatitis (RAP) who have recovered from their attack(s) of AP, whose imaging studies are either normal or show changes consistent with Cambridge classification of 1 or 2, and they have ongoing abdominal pain. Both diabetic and non-diabetic subjects will be allowed to enter the study.
Subjects must be able to read and understand the study information.
Subjects must suffer from abdominal pain suspected to be pancreatic origin with an intensity above 3 on the visual analogue scale (VAS, where 0=no pain and 10= intolerable pain), and meet the criteria for chronic pain (pain ≥ 3 days per week for at least 3 months).
Personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
Subjects willing and able to comply with the scheduled visits, questionnaires, and other study procedures.
Definite Chronic Pancreatitis - Inclusion Criteria
Subjects are 18 years or older in age
Subjects will have a prior confirmed diagnosis of CP on CT scan or MRI/MRCP according to Cambridge Classification (grade 3 or 4). Both diabetic and non-diabetic subjects will be allowed to enter the study.
Subjects must be able to read and understand the study information.
Personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
Subjects willing and able to comply with the scheduled visits, questionnaires, and other study procedures.
Sphincter of Oddi Dysfunction (SOD) Type 1 or Type 2 Inclusion Criteria
Subjects are 18 years or older in age
Subjects have prior diagnosis of Type 1 or Type 2 Sphincter of Oddi Dysfunction (subjects with biliary pain accompanied by biochemical features of transient biliary tract obstruction including elevated transaminases, alkaline phosphatase, or conjugated bilirubin; may also be accompanied by biliary or pancreatic ductal dilation on imaging)
Subjects must be able to read and understand the study information.
Personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
Subjects willing and able to comply with the scheduled visits, questionnaires, and other study procedures.

Exclusion Criteria

Subjects with no pancreatic disease and no abdominal pain, or patients with a diagnosis of functional dyspepsia.
Subjects with evidence or history of medical or surgical disease of importance for this study as judged by investigator.
Subjects suffering from painful conditions that make them unable to distinguish the pain associated with CP from chronic pain of other origins.
Subjects with known pregnancy at the time of enrolment.
Subjects who have previously undergone surgical intervention on their pancreas.
Suspected CPs Exclusion Criteria
Subjects with evidence or history of medical or surgical disease of importance for this study as judged by investigator.
Subjects suffering from painful conditions other than pancreatitis or SOD type 1 or 2 that make them unable to distinguish the pain associated with pancreatitis or SOD from chronic pain of other origins.
Subjects with known pregnancy at the time of enrolment.
Subjects who have previously undergone surgical intervention on their pancreas.
Definite Chronic Pancreatitis Exclusion Criteria
Subjects with evidence or history of medical or surgical disease of importance for this study as judged by investigator.
Subjects suffering from painful conditions other than pancreatitis or SOD type 1 or 2 that make them unable to distinguish the pain associated with pancreatitis or SOD from chronic pain of other origins.
Subjects with known pregnancy at the time of enrolment.
Subjects who have previously undergone surgical intervention on their pancreas.
Sphincter of Oddi Dysfunction (SOD) Type 1 or Type 2 Exclusion Criteria
Subjects with evidence or history of medical or surgical disease of importance for this study as judged by investigator.
Subjects suffering from painful conditions other than pancreatitis or SOD that make them unable to distinguish the pain associated with pancreatitis or SOD from chronic pain of other origins.
Subjects with known pregnancy at the time of enrolment.
Subjects who have previously undergone surgical intervention on their pancreas.

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 Pittsburgh?

Yes, this clinical trial (NCT03434392) has an active research site in Pittsburgh, PA 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.

Chronic Pancreatitis Treatment Options in Pittsburgh, PA

If you're searching for chronic pancreatitis treatment options in Pittsburgh, PA, this clinical trial (NCT03434392) 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 Pittsburgh research site is actively enrolling participants for this clinical trial. You'll receive care from experienced chronic pancreatitis 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 chronic pancreatitis clinical trials near you to find additional studies recruiting in your area.

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