Augusta, GANCT06406790Now EnrollingIRB Ready

Brain Surgery Clinical Trial in Augusta, GA

Access cutting-edge brain surgery treatment through this phase 4 clinical trial at a research site in Augusta. Study-provided care at no cost to qualified participants.

Sponsored by Pramand LLC

Quick Self-Assessment

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Preparing your pre-screening questions…

Expert Care in Augusta

Access brain surgery specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related brain surgery treatment provided free

Apply for This Augusta Location

Check if you qualify for this brain surgery clinical trial in Augusta, GA

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Augusta

    Convenient for GA 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 Augusta site if eligible
  4. 4Begin participation

About This Brain Surgery Study in Augusta

To collect post-approval data comparing the safety and effectiveness of CraniSeal Dural Sealant to DuraSeal Dural Sealant. The study has been powered specifically to determine whether the CraniSeal device when used as an adjunct to sutured dural closure following elective cranial surgery is no worse than (i.e., non-inferior) to the DuraSeal device with respect to proportion of subjects free from post-operative cerebrospinal fluid (CSF) leaks. Additional safety outcomes (i.e., surgical site infec

Sponsor: Pramand LLC

Who Can Participate

Inclusion Criteria

Patient is ≥ 18 years of age
Patient is scheduled for an elective infratentorial or supratentorial cranial procedure under general anesthesia that entails a dural incision
Patient requires a procedure involving surgical wound classification Class I/Clean
Patient signs a written Informed Consent form to participate in the study, prior to any study mandated determinations or procedures.
Patients who are able to comply with study requirements. General

Exclusion Criteria

Patient requires a procedure involving translabyrinthine, transsphenoidal, transoral and/ or any procedure that penetrates the air sinus or mastoid air cells; superficial penetration of air cells are not excluded
Patient has had a prior intracranial neurosurgical procedure in the same anatomical location
Patient with diagnosis of severely altered renal (creatinine levels \> 2.0 mg/dL) or hepatic (total bilirubin \> 2.5 mg/dL) function
Patient diagnosed with a compromised immune system or autoimmune disease (WBC count less than 4000/uL or greater than 20,000/uL)
Patients undergoing cranial procedures involving petrous bone drilling
Patients with traumatic injuries to the head or dural disease in planned dural closure area
Patients who are pregnant or lactating
Patient with an active infection
Patient is undergoing cranial procedures involving non-autologous duraplasty material that are not collagen based
Patients requiring re-opening of planned surgical area within 90 days after surgery.
Patient with a known allergy to FD\&C Blue #1 dye
Patient is not able to tolerate multiple Valsalva maneuvers, or transient elevation of CSF pressure during Valsalva maneuvers is not possible (e.g. the presence of a temporary or permanent CSF shunt
Presence of hydrocephalus
Patient with a diagnosis of uncontrolled diabetes (e.g., persistent HbA1c elevation of \>9% despite standard diabetes care),
Patient has a documented, uncorrectable clinically significant coagulopathy (e.g., PTT\>37 seconds or INR \>1.5 units)
Patient is not likely to comply with the follow-up evaluation schedule.
Contraindications to both an MRI and CT scan.
Patients participating in any investigational device study within 30 days or currently receiving an investigational drug/biologic therapy. (Observational studies on FDA approved products are not applicable)
Patients diagnosed with Meningiomatosis (multiple meningiomas)

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 Augusta?

Yes, this clinical trial (NCT06406790) has an active research site in Augusta, GA 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.

Brain Surgery Treatment Options in Augusta, GA

If you're searching for brain surgery treatment options in Augusta, GA, this clinical trial (NCT06406790) 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 Augusta research site is actively enrolling participants for this phase 4 clinical trial. You'll receive care from experienced brain surgery 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 brain surgery clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Augusta, GA