Evidence map›Paper›PMID 33654425›Full record

ArticleJournal of pain research2021

Open-Label Adhesion Performance Studies of a New Lidocaine Topical System 1.8% versus Lidocaine Patches 5% and Lidocaine Medicated Plaster 5% in Healthy Subjects.

Jeffrey Gudin, Lynn R Webster, Emileigh Greuber, Kip Vought, Kalpana Patel, Louis Kuritzky

3 registry-linked trialsAbstract read
In one paragraph

Article in Journal of pain research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04312750 phase1completednot on this map

An Open Label, Single-treatment, Single-period, Single-application, Adhesion Performance Study of Lidocaine Patch 36 mg/Patch (1.8%) in Healthy, Adult, Human Subjects.

TypeinterventionalSponsorScilex Pharmaceuticals, Inc.Ran2015 to 2015Enrolled54ConditionsHealthyArmsLidocaine topical system 1.8%
NCT04319926 phase1completednot on this map

An Open Label, Randomized, Two-treatment, Two-period, Single-dose Study Evaluating the Product Adhesion in Healthy, Adult Subjects Using ZTlido 1.8% Topical System and a Generic Lidocaine Patch 5%.

TypeinterventionalSponsorScilex Pharmaceuticals, Inc.Ran2018 to 2018Enrolled24ConditionsHealthyArmslidocaine topical system 1.8%, lidocaine patch 5%
NCT04320173 phase1completednot on this map

An Open Label, Three-period, Single-application, Adhesion Performance Study ZTlido® (Lidocaine Topical System) 1.8% Compared to Lidoderm® (Lidocaine Patch 5%) and Versatis® (Lidocaine Medicated Plaster 5%) in Healthy, Adult, Human Subjects

TypeinterventionalSponsorScilex Pharmaceuticals, Inc.Ran2017 to 2017Enrolled47ConditionsHealthyArmsLidocaine patch 1.8%, Lidocaine patch 5%, Lidocaine medicated plaster 5%
3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jeffrey GudinDepartment of Anesthesiology, Rutgers New Jersey Medical School, Newark, NJ, USA.
Lynn R WebsterScientific Affairs Neurosciences, PRA Health Sciences, Salt Lake City, UT, USA.
Emileigh GreuberGlobal Research and Development and Medical Affairs, Scilex Pharmaceuticals Inc, Palo Alto, CA, USA.ORCID 0000-0001-6450-1988
Kip VoughtGlobal Research and Development and Medical Affairs, Scilex Pharmaceuticals Inc, Palo Alto, CA, USA.
Kalpana PatelGlobal Research and Development and Medical Affairs, Scilex Pharmaceuticals Inc, Palo Alto, CA, USA.
Louis KuritzkyCommunity Health and Family Medicine, University of Florida Community Health & Family Medicine, Gainesville, FL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe primary objective was to evaluate adhesion performance of the lidocaine topical system 1.8% for 12 hours in healthy human subjects in three studies: as a single product (Study 1) and versus other lidocaine topical products (lidocaine patch 5% and lidocaine medicated plaster 5% [Study 2] and generic lidocaine patch 5% [Study 3]). Safety of the lidocaine topical system 1.8%, with a skin irritation focus, was a secondary objective. PATIENTS AND

methodsAll three studies were open-label, randomized, Phase 1 adhesion performance studies in healthy adult volunteers (N=125). Lidocaine topical products were applied for 12 hours per test, per study arm. Adhesion of all test products was scored at 0, 3, 6, 9, and 12 hours post-application. Skin irritation was scored after product removal or when a product detached.

resultsOverall, the majority (≥75%) of subjects treated with the lidocaine topical system 1.8% demonstrated ≥90% adhesion (FDA adhesion score 0) throughout the 12-hour administration period versus 13.6% of subjects treated with lidocaine patch 5%, 15.9% of subjects treated with lidocaine medicated plaster 5%, and 0% of subjects treated with the generic lidocaine patch 5%. There were no complete detachments with the lidocaine topical system 1.8%, whereas 4.5% of lidocaine patch 5% and lidocaine medicated plaster 5% detached, and 29% of generic lidocaine patch 5% detached. Minimal skin irritation was observed with each lidocaine topical product.

conclusionAcross three studies, lidocaine topical system 1.8% demonstrated superior adhesion performance versus the three other products tested. Skin irritation was minimal across products and studies. CLINICALTRIALSGOV: NCT04312750, NCT04320173, NCT04319926.

Indexed as

adhesionlidocaine medicated plasterlidocaine patchlidocaine topical systempostherpetic neuralgia

Identifiers

PMID33654425
PMCPMC7914064

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.