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RecruitingNCT06008795BLOCK-SAHUpdated Jul 6, 2026

BLOCK-SAH - PPF-Block for Post-SAH Headache

A Phase 2 interventional study of Pterygopalatine Fossa Nerve Block with Ropivacaine and Dexamethasone and Placebo Pteryogpalatine Fossa Injection in Subarachnoid Hemorrhage, Aneurysmal and Headache, sponsored by University of Florida. Recruiting at 13 sites in United States. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2026-07-06.

Sponsored by University of Florida · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
195
Allocation
Randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

BLOCK-SAH is a phase II, multicenter, randomized, double-blinded, placebo-controlled clinical trial with a sequential parallel comparison design (SPCD) of bilateral pterygopalatine fossa (PPF) injections with 20mg ropivacaine + 4mg dexamethasone (active, PPF-block) compared to saline (placebo) for headache in survivors of aneurysmal subarachnoid hemorrhage (SAH), while monitoring intracranial arterial mean flow velocities with transcranial Doppler (TCD) peri-intervention (intervention = PPF-injections: active or placebo)

02

Conditions studied

  • Subarachnoid Hemorrhage, Aneurysmal
  • Headache

Keywords

  • Pterygopalatine Fossa Nerve Block
03

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

  1. Provision of signed and dated ICF by participant or a legally authorized representative (LAR)
  2. Stated willingness to comply with all study procedures and availability for the duration of the study
  3. Male or female, aged ≥18 and ≤ 85 years
  4. Admitted with a primary diagnosis of spontaneous, non-traumatic, SAH within 72 hours of ictus hemorrhage
  5. Disease-specific inclusion criteria:

    1. Spontaneous, non-traumatic SAH
    2. Subarachnoid pattern of hemorrhage warranting diagnostic DSA due to involvement of at least one of the following regions: quadrigeminal plate, prepontine cistern, perimesencephalic cistern, Sylvian fissure, or surrounding Circle of Willis
    3. Modified Fisher grade 1-4 (on presentation imaging)
    4. Hunt and Hess 1-3 or World Federation of Neurosurgeons grade 1-4 (on screening, included only if also fulfilling Glasgow Coma Scale verbal subscore ≥4)
    5. Minimum Glasgow Coma Scale verbal subscore of 4 (on screening)
  6. Able to verbalize pain scale scores according to 11-point numeric pain scale

    In order to be enrolled and undergo randomization in this study, an individual must meet all of the additional criteria:

  7. Stabilization period criteria:

    1. A minimum of 4 hours from DSA with clipping or coiling procedure (whenever applicable)
    2. Successful treatment of culprit vascular lesion (i.e., ≥90% obliteration of aneurysm), when applicable
  8. Requiring a minimum of 15mg OME prn for headache analgesia during any 24-hour period during eligibility period

Exclusion Criteria:

An individual who meets any of the following criteria will be excluded from participation in this study:

  1. Premorbid conditions:

    1. Pre-existing neurologic, psychiatric, or other condition that would confound neurologic assessment or would make difficult/impossible to accurately assess neurologic and/or functional outcome
    2. Pre-existing diffuse flow-limiting narrowing of arteries in the Circle of Willis, regardless of etiology (e.g., atherosclerosis, vasculitis, Moya-Moya syndrome)
    3. Prior use of opioid or barbiturate analgesics for at least two-thirds of the days in previous month, regardless of indication
    4. Diagnosis of substance use disorder in the previous year
    5. Infected or wounded skin, or a skin lesion at the site of puncture for PPF- injection
  2. Uncorrected coagulopathy

    1. Platelet count \< 50,000/μL, International Normalized Ratio (INR) > 1.7
    2. Requiring use of systemic anticoagulation and antiplatelet therapy (except for aspirin monotherapy).
  3. SAH-specific:

    1. Head trauma as etiology of SAH
    2. Infection as cause for aneurysm or SAH (i.e., mycotic aneurysms)
    3. Inability to successfully treat culprit vascular lesion
    4. Diffuse vasospasm on pre-enrollment diagnostic CTA or DSA. Vasospasm is defined as moderate-to-severe arterial narrowing on DSA or CTA not attributable to atherosclerosis, catheter-induced spasm, or vessel hypoplasia, as determined by a neuroradiologist or neurointerventionalist
  4. Standard pain regimen conditions

    1. Elevation of hepatic enzymes prohibiting use of scheduled APAP (i.e., AST or ALT > 3x upper limit level)
    2. Chronic liver condition with absolute contra-indication for APAP (even at lower maximum daily doses)
  5. Participation in a concurrent investigational/interventional study (observational studies allowed)
  6. Known to be pregnant, or with a positive pregnancy test
  7. Allergy or intolerance to the medications used in the PPF-block (i.e., ropivacaine, dexamethasone) or standard pain regimen (APAP)
  8. Vulnerable populations such as prisoners and inmates (abiding GCP per the study IRB)
  9. Unable to receive first PPF-injection within 96 hours of ictus hemorrhage
04

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Sequential assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
195 participants (estimated)

Study arms

  • Active comparator
    Group 1 - Active - Active

    Subjects randomized to Group 1 will receive an active PPF nerve block in Stage 1 followed by an active PPF nerve block in Stage 2 of the Double-Blinded Trial Phase

    Drug: Pterygopalatine Fossa Nerve Block with Ropivacaine and Dexamethasone

  • Other
    Group 2 - Placebo - Active

    Subjects randomized to Group 2 will receive a placebo PPF-injection in Stage 1 followed by an active PPF nerve block in Stage 2 of the Double-Blinded Trial Phase

    Drug: Pterygopalatine Fossa Nerve Block with Ropivacaine and Dexamethasone · Procedure: Placebo Pteryogpalatine Fossa Injection

  • Placebo comparator
    Group 3 - Placebo - Placebo

    Subjects randomized to Group 3 will receive a placebo PPF-injection in Stage 1 followed by a placebo PPF-injection in Stage 2 of the Double-Blinded Trial Phase

    Procedure: Placebo Pteryogpalatine Fossa Injection

Interventions

  • DrugPterygopalatine Fossa Nerve Block with Ropivacaine and Dexamethasone

    Each PPF-active nerve block will consist of 20mg (4ml) ropivacaine plus 4mg (1ml) dexamethasone

    Also known as: Pterygopalatine Fossa Nerve Block

  • ProcedurePlacebo Pteryogpalatine Fossa Injection

    Each placebo PPF-injection will consist of 5ml normal saline

05

What researchers measure

Primary outcomes

  1. Primary Efficacy Endpoint

    prn oral morphine equivalent (OME)/day use

    Time frame: within 24 hours after each PPF-injection spanning the 48 hours of double-blinded treatment period

  2. Primary Safety Endpoint

    incidence of radiographic vasospasm

    Time frame: at 48 hours from first PPF-injection (end of double-blinded treatment period)

  3. Primary Tolerability Endpoint

    rate of acceptance of second PPF-injection

    Time frame: at 24 hours following the first PPF-injection

06

Study locations

12 of 13 sites recruiting
  • University of Florida
    Gainesville, Florida 32610, United States
    Recruiting
  • University of Miami
    Miami, Florida 33136, United States
    • Ana Karen Bolaños · Contact · axb2916@med.miami.edu · 305-243-3063
    • Nina Massad, MD · Principal investigator
    Recruiting
  • Cleveland Clinic Foundation Martin Health
    Stuart, Florida 34994, United States
    • Irene Ball · Contact · balli@ccf.org · 772-763-9317
    • Marc Babi, MD · Principal investigator
    Recruiting
  • Emory University
    Atlanta, Georgia 30322, United States
    Recruiting
  • University of Maryland Baltimore
    Baltimore, Maryland 21201, United States
    Recruiting
  • Creighton University Medical Center
    Omaha, Nebraska 68124, United States
    Recruiting
  • University of Rochester Medical College
    Rochester, New York 14642, United States
    Recruiting
  • University of North Carolina
    Chapel Hill, North Carolina 27599, United States
    Recruiting
  • University of Cincinnati
    Cincinnati, Ohio 45267, United States
    • Alexandra Ramirez · Contact · ramiream@ucmail.uc.edu · 513-558-0101
    • Charles Prestigiacomo, MD · Principal investigator
    Recruiting
  • Oregon Health and Sciences University
    Portland, Oregon 97239, United States
    • Sarah Feller · Contact · fellersa@ohsu.edu · 503-494-6233
    • Ines Koerner, MD · Principal investigator
    Recruiting
  • Thomas Jefferson University
    Philadelphia, Pennsylvania 19107, United States
    Not yet recruiting
  • University of Washington
    Seattle, Washington 98104, United States
    • Do Lim · Contact · dolim@uw.edu · 206-744-9389
    • Sarah Wahlster, MD · Principal investigator
    Recruiting
  • Medical College of Wisconsin
    Milwaukee, Wisconsin 53226, United States
    • Jacob Labinski · Contact · jlabinski@mcw.edu · 414-805-2578
    • Tom Aufderheide, MD · Principal investigator
    Recruiting
07

References and documents

Publications

  • Busl KM, Smith CR, Troxel AB, Fava M, Illenberger N, Pop R, Yang W, Frota LM, Gao H, Shan G, Hoh BL, Maciel CB; BLOCK-SAH Investigators. Rationale and Design for the BLOCK-SAH Study (Pterygopalatine Fossa Block as an Opioid-Sparing Treatment for Acute Headache in Aneurysmal Subarachnoid Hemorrhage): A Phase II, Multicenter, Randomized, Double-Blinded, Placebo-Controlled Clinical Trial with a Sequential Parallel Comparison Design. Neurocrit Care. 2025 Feb;42(1):290-300. doi: 10.1007/s12028-024-02078-z. Epub 2024 Aug 13. PubMed 39138719 ↗
08

Registry details

Key details

Study ID
NCT06008795
Lead sponsor
University of Florida
Collaborators
National Institute of Neurological Disorders and Stroke (NINDS), New York University, Massachusetts General Hospital
Responsible party
Sponsor
First posted
Aug 24, 2023
Start date
Dec 17, 2023
Primary completion
Jan 15, 2027 (estimated)
Completion
Feb 28, 2027 (estimated)
Last update
Jul 6, 2026

Study contacts

Yurerkis Montas
Contact
ymontas@partners.org
617-866-9758
Ralisa Pop
Contact
ralisa.pop@neurology.ufl.edu
352-294-5693

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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