Pittsford, NYNCT07216430Now EnrollingIRB Ready

Acute Otitis Media (AOM) Clinical Trial in Pittsford, NY

Access cutting-edge acute otitis media (aom) treatment through this clinical trial at a research site in Pittsford. Study-provided care at no cost to qualified participants.

Sponsored by Serum Life Science Europe GmbH

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Expert Care in Pittsford

Access acute otitis media (aom) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related acute otitis media (aom) treatment provided free

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Check if you qualify for this acute otitis media (aom) clinical trial in Pittsford, NY

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Why Participate?

  • No-Cost Study Care

  • Local to Pittsford

    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 Pittsford site if eligible
  4. 4Begin participation

About This Acute Otitis Media (AOM) Study in Pittsford

The goal of this clinical trial is to evaluate whether the wSp vaccine can prevent nasopharyngeal colonization by pneumococcal bacteria in healthy young children who have received routine PCV15 or PCV20 vaccination. The main questions it aims to answer are: Does wSp vaccine reduce pneumococcal colonization in the nose? Does wSp vaccine safely stimulate the immune system to produce antibodies and protective immune responses? Researchers will compare children receiving two injections of wSp vaccine to those receiving saline placebo to see if wSp vaccine reduces colonization and boosts immunity. Participants will: Receive two injections of either wSp or saline at approximately 7 and 9 months of age. Have blood samples taken at 6 and/or 12 months to measure immune responses. Have nasal swabs collected at several time points and during infections from 6-24 months. Be monitored for ear infections, respiratory illnesses, and other pneumococcal-related infections.

Sponsor: Serum Life Science Europe GmbH

Who Can Participate

Inclusion Criteria

Male or female who is 6 months (- 30 to +75 days) of age at time of enrollment
Healthy subject as established by medical history and clinical examination before entering into the study.
Received 3 doses of PCV15 or PCV20.
Written informed consent obtained from the subject's parent/legal guardian.
Parent/legal guardian able and willing to bring subject to all study visits.

Exclusion Criteria

Has a history of invasive pneumococcal disease (positive blood culture and/or positive cerebrospinal fluid culture).
Known or suspected impairment of immunological function, based on medical history and physical examination.
Has a history of congenital or acquired immunodeficiency.
Chronic administration (defined \> 14 consecutive days) of immunosuppressants or other immune-modifying drugs.
Prior receipt since birth of immunoglobulins and/or any blood products or planned administration during the study period.
Expected to receive systemic corticosteroids within 14 days prior to any dose of study vaccine.
External auditory canal atresia/stenosis.
Has known or history of functional or anatomic asplenia.
Has a bleeding disorder in which intramuscular vaccination would be contraindicated.
Participation in another investigational or interventional trial within the 28-day period before enrollment and during the conduct of the study. Participation in observational studies is permitted.
Direct descendant (child or grandchild) of study site personnel. Temporary exclusion criteria For day of vaccination:
Fever (transcutaneous temperature ≥38.0°C) or acute illness, at investigator's discretion
Has received systemic corticosteroids (equivalent of prednisone \> 0.5 mg/kg/day or equivalent) and not completed this course of treatment at least 30 days prior to the study vaccination. Inhaled, topical, and ophthalmic steroids are allowed.

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 Pittsford?

Yes, this clinical trial (NCT07216430) has an active research site in Pittsford, 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.

Acute Otitis Media (AOM) Treatment Options in Pittsford, NY

If you're searching for acute otitis media (aom) treatment options in Pittsford, NY, this clinical trial (NCT07216430) 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 Pittsford research site is actively enrolling participants for this clinical trial. You'll receive care from experienced acute otitis media (aom) 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 acute otitis media (aom) clinical trials near you to find additional studies recruiting in your area.

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