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Transdermal Microneedle Lignocaine Delivery Versus EMLA Patch for Topical Analgesia Before Venepuncture Procedure To Adults in Clinical Setting

StatusRecruiting
PhasePhase 1/2
Started
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Record History

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  1. Notable Trial status: Not Yet Recruiting to Recruitingv6 Show 6 more changesShow less
    • Primary completion date: Aug 31, 2027 to Dec 11, 2026
    • Study completion date: Oct 31, 2027 to Dec 11, 2026
    • Start date changed from estimate of Jun 1, 2025 to Feb 17, 2025
    • Eligibility criteria expanded, about 16 words
    • Study description shortened, about 6 words
    • Site details revised
  2. Notable Primary completion date: Dec 31, 2026 to Aug 31, 2027
    • Start date: Oct 1, 2024 to Jun 1, 2025
    • Study completion date: Jul 31, 2027 to Oct 31, 2027
    v5
  3. Notable Primary completion date: Dec 11, 2024 to Dec 31, 2026v4 Show 4 more changesShow less
    • Start date: May 2, 2023 to Oct 1, 2024
    • Trial status: Recruiting to Not Yet Recruiting
    • Study completion date: Dec 11, 2024 to Jul 31, 2027
    • Site details revised
  4. Notable Trial status: Not Yet Recruiting to Recruiting
    • Site details revised
    v3
  5. Notable Enrollment target: 77 to 154v2
  6. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Microneedle (MN) is a mimic of a hypodermic needle, composed of hundreds of micron-sized, out-of-plane protrusions, typically arranged in arrays on a patch that can be applied onto the skin. MN can be fabricated from a variety of materials, preferably biocompatible polymers. Maltose, a natural carbohydrate, is a safe and biocompatible product that can be fabricated into MNs that are biodegradable and soluble within several minutes. Besides, local anaesthetic agents such as lignocaine can be impregnated within the MN matrix, facilitating its transdermal delivery more efficiently which results in enhanced efficacy. So far, maltose MN efficacy in enhancing the transdermal drug delivery (TDD) of lignocaine and thus reducing the pain experienced by healthy patients requiring venepuncture prior to routine eye surgeries (phacoemulsification, trabeculectomy etc) has not been extensively studied. Hence, the objectives of this research are: 1) To evaluate the safety profile of lignocaine-embedded microneedle patch as a means of pain reduction in adult patients requiring routine vein-puncturing procedures; 2) To assess the pharmacokinetic (PK) parameters of lignocaine in the systemic circulation when the transdermal lignocaine delivery is enhanced through microneedle usage; 3) To compare the efficacy of lignocaine-embedded microneedle patch with standard 5% Eutectic Mixture of Local Anesthetics (EMLA) dermal patch for pain reduction during venepuncture procedure based on mean changes in VAS scores and skin algesimeter index (pharmacodynamic (PD) study).
Trial Details
NCT Number NCT05694858
Lead Sponsor Universiti Kebangsaan Malaysia Medical Centre
Conditions
(from sponsor)
Glaucoma, Cataract, Ophthalmological Disorder
Related terms Cataract, Eye Diseases, Glaucoma
Enrollment 154 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov