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Chronic HeadacheNCT06077747

Lumbar Vein Embolization for Chronic Headaches With Nutcracker Physiology

A study testing Coil Embolization of the Lumbar Vein in people with Chronic Headache and Nutcracker Phenomenon, Renal, run by Mayo Clinic at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The purpose of this research is to gather information on the safety and feasibility of coiling the lumbar vein for the treatment of chronic headaches in patients with Nutcracker physiology and retrograde lumbar vein flow with epidural venous plexus congestion. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Coil Embolization of the Lumbar Vein
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
4 participants
Where
1 siteUnited States
Study dates
17 Sep 2024to Sep 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Daily headache from onset lasting > 3 months.
  • Headache described as pressure sensation.
  • Headache worsened in the Trendelenburg position.
  • Exposed to CSF pressure/volume lowering medications.
  • Tried 2 of 4 unless contraindications: acetazolamide, methazolamide, indomethacin SR or spironolactone) or CSF volume removal via LP with positive or neutral response.
  • Failed at least 3 typical headache preventative medications from different classes-antidepressants, antiepileptic, blood pressure medications.
Show all 11Show fewer
  • MRI demonstrates that Nutcracker physiology is present.
  • Decreased SMA angle, renal vein narrowing, decreased AMD.
  • Retrograde lumbar vein flow and early EVP enhancement.
  • Ability to understand study procedures and to comply with them for the entire length of the study.
  • Negative pregnancy test.

Who cannot join

  • Evidence of disc edema.
  • Positive urinalysis for hematuria or proteinuria.
  • Abnormal CBC or CMP.
  • MRI, MRA head and neck and MR venogram with a possible secondary causes of headache including space occupying lesions, Chiari malformation, cerebral vein thrombosis, hydrocephalus, dissection, aneurysm etc.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United States1 site, 1 recruiting
  • Mayo Clinic Florida

    Jacksonville, Florida, 32224

    Recruiting

Other trials in United States

About this study

Official title: Lumbar Vein Embolization for the Treatment of Chronic Headache in Patients With Nutcracker Physiology and Retrograde Lumbar Vein Flow With Epidural Venous Plexus Enhancement

The purpose of this research is to gather information on the safety and feasibility of coiling the lumbar vein for the treatment of chronic headaches in patients with Nutcracker physiology and retrograde lumbar vein flow with epidural venous plexus congestion. All patients are extensively evaluated by a headache trained Neurologist confirming high pressure headache refractory to other treatments.

Read the detailed description

This is a feasibility, non-randomized, non-blinded clinical trial enrolling patients who are at least 18 years of age for the treatment of chronic headache in the setting of Nutcracker physiology with retrograde lumbar vein flow and epidural venous plexus enhancement.

Patients are initially evaluated by a fellowship trained headache neurologist to obtain a detailed headache history, VAS score, MIDAS score, and physical examination. They are also evaluated by a neuro ophthalmologist with fundoscopic examination to assess for disc edema. A lab work-up is performed including complete blood count, basic metabolic panel, and microscopic urinalysis. A lumbar puncture and imaging work-up are then obtained as well.

Patients will proceed to an MRI to evaluate for Nutcracker physiology, retrograde lumbar vein flow, and epidural venous plexus enhancement if they meet the following criteria:

  1. Daily headache from onset lasting > 3 months
  2. Headache described as pressure sensation
  3. Headache worsened in the Trendelenburg position
  4. MRI, MRA head and neck and MR venogram negative for possible secondary causes of headache including space occupying lesions, Chiari malformation, cerebral vein thrombosis, hydrocephalus, dissection, aneurysm etc
  5. Transverse sinus stenosis is allowed to proceed
  6. Exposed to CSF pressure/volume lowering medications
  7. Tried 2 of 4 unless contraindications: acetazolamide, methazolamide, indomethacin SR or spironolactone) or CSF volume removal via LP with positive or neutral response
  8. Failed at least 3 typical headache preventative medications from different classes: antidepressants, antiepileptic, and blood pressure If these criteria are met, they will undergo an MRI to evaluate for Nutcracker physiology, retrograde lumbar vein flow, and epidural venous plexus enhancement. For those patients that demonstrate Nutcracker physiology with retrograde lumbar vein flow and EVP enhancement they would be eligible for the clinical trial.

If they are interested in the clinical trial, they will be evaluated in clinic by a fellowship trained interventional radiologist to review the following:

  1. Procedural sedation: moderate sedation versus general anesthesia
  2. Prior contrast allergies
  3. Consent for procedure
  4. Prior to venography the patient is taken off all headache medications for 4 weeks.

For patients that are still eligible and interested they will proceed with venography. Venography involves an evaluation of the left renal vein and left lumbar vein to confirm the findings on the MRI. If catheter-based venography confirms Nutcracker physiology with retrograde lumbar vein flow and epidural venous plexus enhancement they will then enter the clinical trial. Embolization of the lumbar vein will be performed. A follow-up venogram will then be performed to ensure there is no further retrograde lumbar vein flow.

After the embolization patient's will be followed for symptom evaluation at 1,3,7,14, and 28 days after the procedure and then monthly. They will also have a follow-up physical examination at 1 month, 3 months, 6 months and then every 6 months post-procedure. They will be followed for a total of 18 months. Some patients may need follow-up laboratory work-up and MRI post-procedure as standard of care.

Being tested
Coil Embolization of the Lumbar Vein
Medical subject headings
Headache Disorders, Renal Nutcracker Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Coil Embolization of the Lumbar VeinProcedure or surgery

    Catheter based venography will first confirm Nutcracker physiology with retrograde lumbar vein flow and epidural venous plexus congestion. The lumbar vein will then be coil embolized.

Study groups in NCT06077747
Study groupRoleWhat they receive
Coil embolization of lumbar veinExperimentalSubjects with confirmed Nutcracker physiology, retrograde lumbar vein flow, and epidural venous plexus congestion with a high pressure headache will have coil embolization of the lumbar vein.
Receives: Procedure: Coil Embolization of the Lumbar Vein

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in headache pain

    Measured by a visual analogue scale (VAS) where 0 = no pain, 5= moderate pain, 10= worst pain

    Measured: 1,3,7,14, and 28 days after the procedure and then monthly for 17 months

  2. Change in Migraine Disability Assessment

    Measured by the Migraine Disability Assessment Test

    Measured: 1,3,7,14, and 28 days after the procedure and then monthly for 17 months

Secondary outcomes (2)
  1. Adverse Events

    Number of adverse events defined as any unwanted symptom that occurred from embolizing the lumbar vein such as flank pain, proteinuria, hematuria, or pelvic congestion.

    Measured: 1,3,7,14, and 28 days after the procedure and then monthly for 17 months

  2. Serious Adverse Events

    Number of serious adverse events defined as any serious unexpected complication during or after the embolization that would result in death, is life threatening, requires prolonged hospitalization, causes persistent or significant disability or incapacity, or another condition that represents significant hazards.

    Measured: 1,3,7,14, and 28 days after the procedure and then monthly for 17 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Oct 2023
  2. Study start17 Sep 2024
  3. Primary completionSep 2027 (estimated)
  4. Study completionSep 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
4 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06077747
Sponsor's protocol ID
23-004668
Status last verified
Nov 2025
First submitted
5 Oct 2023
Last updated
18 Nov 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Coil Embolization of the Lumbar Vein in people with Chronic Headache and Nutcracker Phenomenon, Renal, run by Mayo Clinic at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 11 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 18 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Julia Santos (904-953-3280, Santos.Julia@mayo.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in headache pain (time frame: 1,3,7,14, and 28 days after the procedure and then monthly for 17 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Nov 2025; AzTrials last refreshed its copy on 1 Nov 2026.

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