Pain Perception: Lidocaine Rate/Temp/Buffer
NCT02823002 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 26
Last updated 2024-03-15
Summary
This study will collect data from multiple academic institutions. The primary objective for part A of this study is to determine the impact of anesthetic injection rate and temperature on pain perception during dermatologic procedures, and the objective for the part B of this study is to determine if buffering of the anesthetic solution alters pain perception.
This study is a pilot study designed to determine feasibility of these procedures.
Conditions
Interventions
- PROCEDURE
-
Slow, Room Temperature Injection
The room temperature local anesthetic agent will be administered by slow infiltration.
- PROCEDURE
-
Rapid, Room Temperature Injection
The room temperature local anesthetic agent will be administered by rapid infiltration.
- PROCEDURE
-
Slow, Warm Temperature Injection
The warmed local anesthetic agent will be administered by slow infiltration.
- PROCEDURE
-
Rapid, Warm Temperature Injection
The warmed local anesthetic agent will be administered by rapid infiltration.
- PROCEDURE
-
Buffered Injection
One side of the body will be randomized to receive an injection of the buffered agent, while the contralateral side will be assigned to receive an injection of the unbuffered anesthetic agent.
- PROCEDURE
-
Non-Buffered Injection
One side of the body will be randomized to receive an injection of the buffered agent, while the contralateral side will be assigned to receive an injection of the unbuffered anesthetic agent.
- DRUG
-
Lidocaine
Injectable lidocaine solution (Lidocaine Hydrochloride and Epinephrine)
- DRUG
-
Buffer
Sodium Bicarbonate
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
Murad Alam, MD · Northwestern University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 89 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2016-06-30
- Primary Completion
- 2025-01-31
- Completion
- 2025-01-31
Countries
- United States
Study Locations
More Related Trials
-
Local Anesthetics for Pain Reduction Prior to IV Line Placement
NCT01759459 ·Status: COMPLETED ·Phase: PHASE4
-
Lidocaine Infusions for Chronic Pain in Children
NCT02983682 ·Status: COMPLETED ·Phase: PHASE3
-
Optimal Lidocaine Buffering to Reduce Injection Pain in Local Anesthesia
NCT02647892 ·Status: TERMINATED ·Phase: PHASE4
-
Kinetic Anesthesia Device Study
NCT03344510 ·Status: COMPLETED ·Phase: NA
-
Reducing Pain of Lidocaine Injection
NCT02288364 ·Status: COMPLETED ·Phase: PHASE4
-
Effect of IV Lidocaine Infusions on Pain
NCT00725504 ·Status: COMPLETED ·Phase: NA
-
Safety of Intravenous Lidocaine Infusions
NCT01091935 ·Status: COMPLETED
-
Effectiveness Study of Different Local Anesthetic Mixtures
NCT01243112 ·Status: COMPLETED ·Phase: PHASE4
-
The Effect of Needle Temperature on Pain Ratings Following Intramuscular Injection
NCT00213967 ·Status: COMPLETED ·Phase: NA
-
Comparison of the Total Dose and Efficacy of Two Lidocaine Concentrations Needed for Cutaneous Surgery Local Anesthesia
NCT00594542 ·Status: COMPLETED ·Phase: NA
-
Lidocaine-Ketamine for Management of Chronic Pain
NCT03249025 ·Status: UNKNOWN ·Phase: NA
-
Injectable Lidocaine Versus Lidocaine/Tetracaine Patch for the Incision and Drainage of Skin Abscesses
NCT02066818 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Effectiveness of 10% Lidocaine on Relieving Pain Caused by Intravenous Intubation
NCT07212192 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Clinical Outcomes of Buffered vs. Non-Buffered Lidocaine
NCT02620683 ·Status: COMPLETED ·Phase: NA
-
Cutaneous Administration of Local Anesthetic for Spine Injection Procedures
NCT00756301 ·Status: COMPLETED ·Phase: NA
-
An Evaluation of the Effectiveness of Local Anesthetics Used During Intravenous Catheter Insertion
NCT02162680 ·Status: COMPLETED ·Phase: PHASE4
-
Lidocaine and Neuroma Pain Related Modalities
NCT02300038 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy of Lidocaine Versus Ketamine Infusion for Resistant Orofacial Pain
NCT07250867 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2
-
Buffered vs. Unbuffered Local Anesthesia in Mandibular Molars Diagnosed With Symptomatic Irreversible Pulpitis
NCT05227300 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy of Injected Local Anesthetic vs Topical Anesthetic in Cosmetic Injectable Fillers.
NCT02379221 ·Status: COMPLETED ·Phase: NA
-
Effect of Pre-Warming of Local Anesthesia in Reducing Pain Perception During Injection in Children
NCT06519838 ·Status: COMPLETED ·Phase: NA
-
Experimental Pain Study to Assess Local Anesthetic Efficacy and Safety of CTY-5339 Anesthetic Spray in Normal Volunteers
NCT02908620 ·Status: COMPLETED ·Phase: PHASE2
-
Local Anesthesia and Pain Perception During an Amniocentesis
NCT00583011 ·Status: COMPLETED ·Phase: NA
-
Lidocaine Analgesia For Removal Of Wound Vac Dressings
NCT01126359 ·Status: COMPLETED ·Phase: NA
-
Effect of Systemic Ropivacaine on Hyperalgesia, Flare Reaction and Peripheral Nerve Excitability
NCT00900913 ·Status: COMPLETED ·Phase: PHASE4