Rochester, MNNCT05116930Now EnrollingIRB Ready

Post-Dural Puncture Headache Clinical Trial in Rochester, MN

Access cutting-edge post-dural puncture headache treatment through this clinical trial at a research site in Rochester. Study-provided care at no cost to qualified participants.

Sponsored by Mayo Clinic

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Expert Care in Rochester

Access post-dural puncture headache specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related post-dural puncture headache treatment provided free

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Check if you qualify for this post-dural puncture headache clinical trial in Rochester, MN

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Why Participate?

  • No-Cost Study Care

  • Local to Rochester

    Convenient for MN 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 Rochester site if eligible
  4. 4Begin participation

About This Post-Dural Puncture Headache Study in Rochester

The purpose of this study is to evaluate Neostigmine and Glycopyrrolate to treat post-dural puncture headache (PDPH) to reduce the proportion of postpartum women with a PDPH requiring epidural blood patch (EBP) who developed a PDPH after accidental dural puncture.

Sponsor: Mayo Clinic

Who Can Participate

Inclusion Criteria

Post-dural puncture headache (PDPH) after documented dural puncture with Tuohy needle during placement of epidural analgesia for labor and no other explanation for headache (HA).
Onset of HA within 72 hours of delivery.

Exclusion Criteria

Patient refusal.
Visual analog scale (NRS) score \< 4.
History of migraine headaches.
Arrhythmia.
Heart block.
Myasthenia gravis.
Inability to understand pain scores and other questionnaires.
Inability to speak English.
Contraindication to acetaminophen or NSAIDs.
Temperature \> 38.5 C.
Prior EBP done for this HA.

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 Rochester?

Yes, this clinical trial (NCT05116930) has an active research site in Rochester, MN 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.

Post-Dural Puncture Headache Treatment Options in Rochester, MN

If you're searching for post-dural puncture headache treatment options in Rochester, MN, this clinical trial (NCT05116930) 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 Rochester research site is actively enrolling participants for this clinical trial. You'll receive care from experienced post-dural puncture headache 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 post-dural puncture headache clinical trials near you to find additional studies recruiting in your area.

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