Baltimore, MDNCT05119842Now EnrollingIRB Ready

Paralysis, Unilateral, Vocal Cord Clinical Trial in Baltimore, MD

Access cutting-edge paralysis, unilateral, vocal cord treatment through this clinical trial at a research site in Baltimore. Study-provided care at no cost to qualified participants.

Sponsored by APrevent Biotech GmbH

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Expert Care in Baltimore

Access paralysis, unilateral, vocal cord specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related paralysis, unilateral, vocal cord treatment provided free

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Why Participate?

  • No-Cost Study Care

  • Local to Baltimore

    Convenient for MD 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 Baltimore site if eligible
  4. 4Begin participation

About This Paralysis, Unilateral, Vocal Cord Study in Baltimore

This is a prospective, 2-part, multi-center, open-label, non-randomized clinical trial to assess safety and effectiveness of APrevent® VOIS Implants for the treatment of patients with Unilateral Vocal Fold Paralysis (UVFP). In total 30 evaluable patients are planned to be enrolled.

Sponsor: APrevent Biotech GmbH

Who Can Participate

Inclusion Criteria

Male and female patients between 18 and 80 years
Diagnosed with permanent UVFP and insufficient glottal closure
A significant voice disorder as measured by perceptual rating (Grade ≥2 GRBAS Scale) and Voice Handicap Index (VHI-30 score \>33)
Ability to comprehend the full nature and purpose of the study, including possible risks and side effects
Ability to co-operate with the Investigator and to comply with the requirements of the entire study
Availability to volunteer for the entire study duration, willing to adhere to all protocol requirements and willing and able to give informed consent for participation

Exclusion Criteria

Any other significant disease or disorder which, in the opinion of the investigator, may either put the participant at risk because of participation in the clinical investigation may influence the result of the clinical investigation, or the participant's ability to participate in the clinical investigation
Scheduled elective surgery or other procedures requiring general anaesthesia during clinical investigation
Bilateral vocal fold paralysis
Had injection medialization laryngoplasty with the injectable still being within the double length of the maximum resorption time frame as stated in their approval or as supported by literature.
Presence of structural vocal fold lesions such as polyp or nodules
Presence of oropharyngeal or laryngeal tumors
Patients with diagnosed severe obstructive sleep apnea (OSA)
Status post total cordectomy
Previous laryngeal framework surgery (any type of thyroplasty, arytenoid adduction)
Status post tracheostomy
Presence of acute systemic infection at time of screening or shortly before surgery
Significant non-laryngeal speech abnormality (severe dysarthria determined by a panel of trained speech therapists)
Severe coagulopathy
Females who are pregnant, lactating or planning pregnancy are excluded from the investigation
Patients with bil. Gr. III-IV hypertrophic tonsils
Diabetes mellitus with poor control and poor wound healing history

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 Baltimore?

Yes, this clinical trial (NCT05119842) has an active research site in Baltimore, MD 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.

Paralysis, Unilateral, Vocal Cord Treatment Options in Baltimore, MD

If you're searching for paralysis, unilateral, vocal cord treatment options in Baltimore, MD, this clinical trial (NCT05119842) 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 Baltimore research site is actively enrolling participants for this clinical trial. You'll receive care from experienced paralysis, unilateral, vocal cord 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 paralysis, unilateral, vocal cord clinical trials near you to find additional studies recruiting in your area.

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