5% Lidocaine-medicated Plaster for the Treatment of Trigeminal Neuralgia
NCT04570293 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 226
Last updated 2023-03-14
Summary
Trigeminal neuralgia (TN) is characterized by sudden, severe, usually unilateral, transient, stinging, recurrent electrocute-like shock in one or more divisions of the trigeminal nerve, lasting from a few seconds to less than 2 minutes.Simple daily-life activities, such as washing the face, brushing the teeth, eating, and talking, or the slight touch of trigger points may trigger the attack of pain of TN, resulting in a decline in the patient's quality of life (QoL). Trigger zones predominantly locate in the perioral and nasal region. Paroxysmal pain is associated with triggers in virtually all patients with TN. TN may be caused by abnormality of the trigger zone and the blockade of Na+ channel of trigger zone may be a novel and effective treatment methods for TN. Currently, most patients with TN may not achieve adequate pain relief with a single therapeutic agent. Multiple analgesics targeting different mechanisms of the pain pathway are often used.5% lidocaine medicated plaster (LMP) is a white hydrogel plaster containing adhesive material. LMP was approved for post-herpetic neuralgia (PHN) treatment by the United States Food and Drug Administration (FDA) in 1999. Tamburin et al reported that 2 patients with primary TN who stopped oral drugs because of side effects or refused surgical procedures. Both patients were instructed to wear LMP over the affected area and LMP resulted in reduction of pain intensity and the number of pain paroxysms without side effects. However, due to limitations of these open-label design studies, the observed reductions in pain intensity may have been due to treatment effect, placebo effect, changes in underlying disease state, or a combination of these factors. Therefore, randomized controlled trials will be need to be performed to draw about the efficacy of the LMP in TN.
The PATCH trial is a prospective, double-blinded, vehicle-controlled, parallel-group, multicenter, enriched enrolment with randomized withdrawal (EERW) trial aimed at estimating the efficacy and safety of LMP in patients with TN. After providing informed consent and completing a baseline evaluation, patients will participate in an initial open-label treatment period of LMP (active patches). This openly titrated process is close to clinical practice and can provide data on the proportion of responders and non-responders, the optimal dose of the analgesic drug, and the proportion of withdrawal due to adverse effects. A responder at the end of the open-label treatment phase will be included in the subsequently double-blind treatment phase.
Conditions
- Trigeminal Neuralgia
Interventions
- DRUG
-
5% lidocaine medicated plaster
The 5% lidocaine medicated plaster is measuring 10 cm x 14 cm contains 700 mg lidocaine (5% w/w) For each patient, the painful area and the trigger point will be chosen for treatment. The investigator will instruct the patient to replace the patch every 12 hours. The patches could be applied during the night (application in the evening and removal in the morning), or during the day. Patients will be told to apply up to three patches at one time.
- DRUG
-
vehicle plaster
Vehicle patches are identical to the active patch, except for the absence of lidocaine, without any optical differences.For each patient, the painful area and the trigger point will be chosen for treatment. The investigator will instruct the patient to replace the patch every 12 hours. The patches could be applied during the night (application in the evening and removal in the morning), or during the day. Patients will be told to apply up to three patches at one time.
Sponsors & Collaborators
-
Beijing Tiantan Hospital
lead OTHER
Principal Investigators
-
Fang Luo · Beijing Tiantan Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-05-01
- Primary Completion
- 2022-08-26
- Completion
- 2022-08-26
Countries
- China
Study Locations
More Related Trials
-
Tetracaine Compared to Placebo for Reducing Pain With Palivizumab - A Pilot Study
NCT00484393 ·Status: COMPLETED ·Phase: PHASE4
-
A Study of the Use of Microneedle Patches to Deliver Topical Lidocaine in the Oral Cavity
NCT03629041 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetic Study of Lidocaine Patch 1.8% Lidocaine Patch 5% (Lidoderm®) in Healthy Subjects
NCT04144192 ·Status: COMPLETED ·Phase: PHASE1
-
The Effect of Buccal Infiltration Administration of Clonidine on the Success Rate of Inferior Alveolar Nerve Block
NCT04186299 ·Status: WITHDRAWN ·Phase: PHASE4
-
Effect of Sodium Bicarbonate Buffered Lidocaine on the Success of IAN Block of Teeth With Irreversible Pulpitis
NCT02226913 ·Status: COMPLETED ·Phase: PHASE3
-
Evaluation of the Effect of Adding Dexamethasone to 2% Lidocaine
NCT05361291 ·Status: COMPLETED ·Phase: NA
-
Lidocaine and Tetracaine Cream to Treat Postherpetic Neuralgia (PHN)
NCT00609323 ·Status: COMPLETED ·Phase: PHASE2
-
Study Evaluating Heated Lidocaine/Tetracaine Patch in Patients With Pain Associated With Myofascial Trigger Points
NCT01106989 ·Status: COMPLETED ·Phase: PHASE2
-
Pre Injection Use of Cryoanesthesia Versus Topical Anesthetic Gel in Reducing Pain Perception During Palatal Injections
NCT06165432 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy of Dexamethasone or Adrenaline in Inferior Alveolar Nerve Block
NCT04850885 ·Status: COMPLETED ·Phase: PHASE3
-
Pain Assessment During Mandibular Nerve Block Injection With the Aid of Dental Vibe Tool in Pediatric Dental Patients
NCT03790540 ·Status: COMPLETED ·Phase: PHASE2
-
Comparative Pharmacokinetic Study of Lidocaine Patch 1.8% (ZTlido™) and Lidocaine Patch 5% (Lidoderm®) in Healthy Subjects
NCT04149938 ·Status: COMPLETED ·Phase: PHASE1
-
Lidocaine and Neuroma Pain Related Modalities
NCT02300038 ·Status: COMPLETED ·Phase: NA
-
Effect of Lidocaine/Dexamethasone on the Success of IANB
NCT03531970 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Evaluation of the Depth and Duration of Anesthesia From Heated Lidocaine/Tetracaine (Synera®) Patches Compared With 5% Lidocaine (Lidoderm®) Patches Applied to Healthy Adult Volunteers
NCT01688518 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics and Adhesion of Lidocaine Topical System 1.8% Under Conditions of Heat and Exercise
NCT04150536 ·Status: COMPLETED ·Phase: PHASE1
-
Study Evaluating a Heated Lidocaine and Tetracaine Topical Patch in the Treatment of Patients With Patellar Tendinopathy
NCT01111773 ·Status: COMPLETED ·Phase: PHASE2
-
Topical Lidocaine for Needle Insertion and Injection Pain
NCT03206320 ·Status: COMPLETED ·Phase: NA
-
PK and DPK of Lidocaine Dermal Products
NCT03145207 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
The Influence of Intravenous Lidocaine on the Action of the Neuromuscular Blocker Rocuronium
NCT00828373 ·Status: COMPLETED ·Phase: PHASE4
-
Comparison of the Effects of Vapocoolant Spray and EMLA Cream on Pain During Needle Electromyography
NCT01606046 ·Status: COMPLETED ·Phase: PHASE4
-
Comparison of Two Topical Anesthetics: Benzocaine Versus Pliaglis
NCT01951820 ·Status: COMPLETED ·Phase: PHASE4
-
Adhesion Performance Study of Lidocaine Topical System 1.8% Compared to Lidocaine Patch 5% and Lidocaine Medicated Plaster 5% in Healthy, Adult, Human Subjects
NCT04320173 ·Status: COMPLETED ·Phase: PHASE1
-
Duration of Skin Numbing Effect Created by the S-Caine™ Peel
NCT00110253 ·Status: COMPLETED ·Phase: PHASE3
-
Evaluate the Depth and Duration of Anesthesia
NCT00891163 ·Status: COMPLETED ·Phase: PHASE4