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Lumbar Vein Embolization for Chronic Headaches With Nutcracker Physiology

Primary Purpose

Chronic Headache, Nutcracker Phenomenon, Renal, Nutcracker Syndrome, Renal

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Coil Embolization of the Lumbar Vein
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Headache

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 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. 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. Exclusion Criteria: 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.

Sites / Locations

  • Mayo Clinic Florida

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Coil embolization of lumbar vein

Arm Description

Subjects 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.

Outcomes

Primary Outcome Measures

Change in headache pain
Measured by a visual analogue scale (VAS) where 0 = no pain, 5= moderate pain, 10= worst pain
Change in Migraine Disability Assessment
Measured by the Migraine Disability Assessment Test

Secondary Outcome Measures

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.
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.

Full Information

First Posted
October 5, 2023
Last Updated
October 5, 2023
Sponsor
Mayo Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT06077747
Brief Title
Lumbar Vein Embolization for Chronic Headaches With Nutcracker Physiology
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
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
December 2023 (Anticipated)
Primary Completion Date
May 2024 (Anticipated)
Study Completion Date
May 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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. All patients are extensively evaluated by a headache trained Neurologist confirming high pressure headache refractory to other treatments.
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: Daily headache from onset lasting > 3 months Headache described as pressure sensation Headache worsened in the Trendelenburg position 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 a. Transverse sinus stenosis is allowed to proceed Exposed to CSF pressure/volume lowering medications a. 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, 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: Procedural sedation: moderate sedation versus general anesthesia Prior contrast allergies Consent for procedure 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Headache, Nutcracker Phenomenon, Renal, Nutcracker Syndrome, Renal

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
4 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Coil embolization of lumbar vein
Arm Type
Experimental
Arm Description
Subjects 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.
Intervention Type
Procedure
Intervention Name(s)
Coil Embolization of the Lumbar Vein
Intervention Description
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.
Primary Outcome Measure Information:
Title
Change in headache pain
Description
Measured by a visual analogue scale (VAS) where 0 = no pain, 5= moderate pain, 10= worst pain
Time Frame
1,3,7,14, and 28 days after the procedure and then monthly for 17 months
Title
Change in Migraine Disability Assessment
Description
Measured by the Migraine Disability Assessment Test
Time Frame
1,3,7,14, and 28 days after the procedure and then monthly for 17 months
Secondary Outcome Measure Information:
Title
Adverse Events
Description
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.
Time Frame
1,3,7,14, and 28 days after the procedure and then monthly for 17 months
Title
Serious Adverse Events
Description
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.
Time Frame
1,3,7,14, and 28 days after the procedure and then monthly for 17 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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. 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. Exclusion Criteria: 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kendra Brown
Phone
904-953-7755
Email
Brown.Kendra@mayo.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zlatko Devcic, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic Florida
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32224
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
https://www.mayo.edu/research/clinical-trials
Description
Mayo Clinic Clinical Trials

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Lumbar Vein Embolization for Chronic Headaches With Nutcracker Physiology

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