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WithdrawnNCT02955524TOPIACUpdated Apr 20, 2018

Topical Anesthesia and Intra-arterial Chemotherapy for Retinoblastoma

An Early Phase 1 interventional study of Tetracaine 0.5% and Lidocaine hydrochloride ophthalmic gel 3.5% in Hemodynamic Instability, sponsored by University of Miami. Withdrawn. Open to participants aged 8 Weeks and older. Per ClinicalTrials.gov, last updated 2018-04-20.

Sponsored by University of Miami · Early Phase 1, Interventional, and Prevention

Why this study was withdrawn
I discontinued this study because I transferred to another institution.
Phase
Early Phase 1
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
8 Weeks and older
Sex
All
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Study summary

The objective of this study is to use local topical anesthesia to numb the sensory input, captured by branches of the Trigeminal nerve found on the skin in and around the eye, to decrease a hemodynamic reflex seen during placement of a catheter for intra-arterial chemotherapy (IAC) for eye tumors in children. This Trigeminal-cardiac reflex brings about hemodynamic instability during general anesthesia.

Normally, one could block this sensorial input with ophthalmic peribulbar placement of local anesthetics, but these eyes have malignant growth and invasive procedures may cause more harm. The investigators are aiming to numb the sensory branches of the trigeminal nerve non-invasively and observe for any decrease in these events.

Read the detailed description

Retinoblastoma is a rare tumor of the eye and accounts for 6% of malignancies in children less than 5 years of age. Pediatric anesthesiologists have observed a series of hemodynamic instability following the insertion of a catheter into the cavernous segment of the internal carotid artery or during manipulation of a micro-catheter into the ophthalmic artery for intra-arterial chemotherapy (IAC) of retinoblastoma cases by neuroradiologists. This reaction has been recently published in case reports and observational studies as the treatment of these tumors have moved into the interventional imaging suites. This reaction closely resembles the "diving reflex" seen when a person is submerged in cold water; known as the trigeminal-cardiac reflex. It manifests as a sudden hemodynamic disturbance in arterial blood pressure, heart rate, arrhythmia and changes in pulmonary compliance.Rescue from a trigeminal-cardiac reflex entails increasing intravascular volume, administrating mild to resuscitative doses of epinephrine and ventilatory support.

Catheter manipulation around the ophthalmic artery can stimulate the afferent pathway of the trigeminal nerve, branches V1 and V2, originating around the eye to be treated.The ethmoidal nerve, from the nasal passage on the same side, is also stimulated. This in turn triggers a response by the vagus nerve with hemodynamic instability.

Method: Participants are placed under general endotracheal anesthesia for this scheduled procedure. One drop of ocular antiseptic (betadine 5%) will be placed in the eye to be treated followed by a drop of topical FDA approved local anesthetic, Tetracaine 0.5%, to the nasolacrimal duct ( inner corner of the eye) on the eye to be treated. This will numb the ethmoidal nerve in the nasal passage. This is followed by 1 ml of 3.5% Lidocaine gel to the surface of the eye. This gel is placed on the surface of the eye and skin around the eye to numb V1 and V2 fibers of the trigeminal nerve. The study will observe if there is any decrease in the intensity of the reflex or incidence of the reflex during placement of the micro-catheter.

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Conditions studied

  • Hemodynamic Instability

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03

In context

Retinoblastoma

124 studies on the registry are indexed under Retinoblastoma; 23 are open to participants now.

Browse Retinoblastoma studies →

Lead sponsor

University of Miami is the lead sponsor of 820 studies on the registry; 161 are open to participants now.

Of its 111 completed or terminated interventional studies of FDA-regulated products, 93 (84%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
8 Weeks and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Children with Retinoblastoma diagnosis scheduled for Intra-arterial chemotherapy under general anesthesia

Exclusion criteria

Exclusion Criteria:

  • any candidate with history of allergy to anesthetics or preservatives used in local anesthetics any candidate that has a history of allergic dermatitis any candidate that has an open wound in and around the eye to be treated
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Study design

Phase
Early Phase 1
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Treatment session 1a

    Topical ophthalmic anesthesia to participants (#) on each session (letter) of intra-arterial chemotherapy. where #1 is the participant identifier and letter-a is the start session with study protocol (most candidates will receive more than 4 sessions in a 6 month period)

    Drug: Tetracaine 0.5% · Drug: Lidocaine hydrochloride ophthalmic gel 3.5%

Interventions

  • DrugTetracaine 0.5%

    One drop of 0.5% Proparacaine to nasolacrimal Duct to numb the ethmoidal nerve in the nasal passage on the side of the eye to be treated.

  • DrugLidocaine hydrochloride ophthalmic gel 3.5%

    1ml of lidocaine gel is placed over the conjunctivae of the eye to be treated after the patient is under general anesthesia and before the procedure

    Also known as: Akten

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What researchers measure

Primary outcomes

  1. Decrease in systolic Blood Pressure

    Interventionalist will communicate to the investigator of the catheter placement and our outcome measure will be recorded soon after.

    Time frame: 5 seconds

  2. Drop in end-tidal C02

    Interventionalist will communicate to the investigator of the catheter placement and our outcome measure will be recorded soon after.

    Time frame: 5 seconds

  3. Decrease in lung compliance

    Interventionalist will communicate to the investigator of the catheter placement and our outcome measure will be recorded soon after.

    Time frame: 5 seconds

  4. Decrease in oxygen saturation

    Interventionalist will communicate to the investigator of the catheter placement and our outcome measure will be recorded soon after.

    Time frame: 5 seconds

  5. Cardiac arrythmia

    Interventionalist will communicate to the investigator of the catheter placement and our outcome measure will be recorded soon after.

    Time frame: 5 seconds

Secondary outcomes

  1. Recovery from Trigeminal-cardiac event

    Investigator will communicate when the event is over or rescue drugs given.

    Time frame: 2 minutes

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Study locations

No study locations are listed for this record.

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References and documents

Publications

  • Scharoun JH, Han JH, Gobin YP. Anesthesia for Ophthalmic Artery Chemosurgery. Anesthesiology. 2017 Jan;126(1):165-172. doi: 10.1097/ALN.0000000000001381. No abstract available. PubMed 27748655 ↗
  • Jabbour P, Chalouhi N, Tjoumakaris S, Gonzalez LF, Dumont AS, Chitale R, Rosenwasser R, Bianciotto CG, Shields C. Pearls and pitfalls of intraarterial chemotherapy for retinoblastoma. J Neurosurg Pediatr. 2012 Sep;10(3):175-81. doi: 10.3171/2012.5.PEDS1277. Epub 2012 Jul 13. PubMed 22793160 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 20, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02955524
Lead sponsor
University of Miami
Responsible party
Jacqueline L Tutiven (Assistant Professor of Clinical Anesthesiology/Pediatric Anesthesia Dir., University of Miami) — Principal investigator
First posted
Nov 4, 2016
Start date
Mar 2018 (estimated)
Primary completion
Jun 2020 (estimated)
Completion
Dec 2020 (estimated)
Last update
Apr 20, 2018

Study contacts

Jacqueline Tutiven, MD
principal investigator · Director Pediatric Anesthesia Fellowship/Assistant Professor
Norman Halliday, MD
study chair · Chief, Pediatric Anesthesiology

Oversight

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

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This study is withdrawn, as verified in Apr 2018. You cannot join it, but the record below documents what was studied.

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