The Bronx, NYNCT05851976Now EnrollingIRB Ready

Back Pain, Low Clinical Trial in The Bronx, NY

Access cutting-edge back pain, low treatment through this phase 4 clinical trial at a research site in The Bronx. Study-provided care at no cost to qualified participants.

Sponsored by Montefiore Medical Center

Quick Self-Assessment

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Expert Care in The Bronx

Access back pain, low specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related back pain, low treatment provided free

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Check if you qualify for this back pain, low clinical trial in The Bronx, NY

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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 The Bronx

    Convenient for NY 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 The Bronx site if eligible
  4. 4Begin participation

About This Back Pain, Low Study in The Bronx

This research study will help determine whether a medication called duloxetine can improve back pain. It is well documented that many participants who come to the ER with acute low back pain still have low back pain 3 months later. The investigator team will attempt to determine whether duloxetine can help prevent this.

Sponsor: Montefiore Medical Center

Who Can Participate

Inclusion Criteria

Present to Emergency Department (ED) primary for management of LBP, defined as pain originating between the lower border of the scapulae and the upper gluteal folds. Flank pain, that is pain originating from tissues lateral to the paraspinal muscles, will not be included.
Musculoskeletal etiology of low back. Patients with non-musculoskeletal etiologies such as urinary tract infection, ovarian cysts, or influenza like illness will be excluded. The primary clinical diagnosis, at the conclusion of the ED visit, must be a diagnosis consistent with non-traumatic, non-radicular, musculoskeletal LBP.
Patient is to be discharged home. Patients admitted to the hospital are more likely to be treated with parenteral medication and therefore are not appropriate for this study.
Age 18-64 Enrollment will be limited to adults younger than 65 years because of the increased risk of adverse medication effects in older patients.
Non-radicular pain. Patients will be excluded if the pain radiates below the gluteal folds in a radicular pattern.
Pain duration \<2 weeks (336 hours).
Prior to the acute attack of LBP, back pain cannot occur more frequently than once per week.
Functionally impairing back pain: A baseline score of \> 5 on the Roland-Morris Disability Questionnaire

Exclusion Criteria

Not available for follow-up
Pregnant or breast-feeding
Chronic pain syndrome defined as moderate or severe pain anywhere in their body on \>= 50% of days for at least three months
Allergic to or intolerant of investigational medications
Contra-indications to non-steroidal anti-inflammatory drugs:
history of hypersensitivity to NSAIDs or aspirin
active or history of peptic ulcer disease, chronic dyspepsia, or active or history of gastrointestinal bleed
Severe heart failure (NYHA 2 or worse)
uncontrolled blood pressure (\>160/100)
Glomerular Filtration Rate (GFR) \<60ml/min
Current use of anti-coagulants
cirrhosis or acute hepatitis
Contra-indication to duloxetine:
alcohol use disorder
chronic liver disease
chronic kidney disease
Active use of medication for depression
Score \> 10 on the Patient Health Questionnaire (PHQ-9) screening instrument or thoughts of suicide, symptoms of feeling down, depressed, or hopeless PHQ9 score \>4. Now we would like to exclude patients with a PHQ9 score \>10 or symptoms of feeling down, depressed, or hopeless

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 The Bronx?

Yes, this clinical trial (NCT05851976) has an active research site in The Bronx, NY 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.

Back Pain, Low Treatment Options in The Bronx, NY

If you're searching for back pain, low treatment options in The Bronx, NY, this clinical trial (NCT05851976) 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 The Bronx research site is actively enrolling participants for this phase 4 clinical trial. You'll receive care from experienced back pain, low 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 back pain, low clinical trials near you to find additional studies recruiting in your area.

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