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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04167189
Other study ID # 2019-01A
Secondary ID
Status Completed
Phase Early Phase 1
First received
Last updated
Start date January 20, 2018
Est. completion date March 30, 2020

Study information

Verified date June 2021
Source PhenoSolve, LLC
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This work will assess the prevalence in hard-to-treat ADHD of the ineffectiveness of the anesthetic Lidocaine.


Description:

Using a non-invasive, pain-free, taste-based approach to assess lidocaine effectiveness, the study will assess the frequency of ineffectiveness in the target population.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date March 30, 2020
Est. primary completion date March 30, 2020
Accepts healthy volunteers No
Gender All
Age group 7 Years to 49 Years
Eligibility Inclusion Criteria: ADHD Exclusion Criteria for both arms: 1. known adverse reactions to lidocaine 2. epilepsy, IQ <80, severe head trauma, birth weight <2270 grams, and severe autism; 3. treatment currently with potassium or potassium-elevating drugs such as renin-angiotensin-aldosterone blockers; 4. generalized anxiety disorders (but dental-specific anxiety will not be an exclusion because many of these individuals may be ones with anxiety because of painful dental experiences with lidocaine ineffectiveness); 5. mouth sores; 6. Ehlers Danlos syndrome, and 7. red hair.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Lidocaine gel
Septodont 5% oral lidocaine gel (NDC 0362-0221-10), 75 mg

Locations

Country Name City State
United States NeurAbilitis Voorhees New Jersey

Sponsors (2)

Lead Sponsor Collaborator
PhenoSolve, LLC NeurAbilities (formerly CRCNJ)

Country where clinical trial is conducted

United States, 

References & Publications (7)

Infante MA, Moore EM, Nguyen TT, Fourligas N, Mattson SN, Riley EP. Objective assessment of ADHD core symptoms in children with heavy prenatal alcohol exposure. Physiol Behav. 2015 Sep 1;148:45-50. doi: 10.1016/j.physbeh.2014.10.014. Epub 2014 Oct 23. — View Citation

Levitt JO. Practical aspects in the management of hypokalemic periodic paralysis. J Transl Med. 2008 Apr 21;6:18. doi: 10.1186/1479-5876-6-18. Erratum in: J Transl Med. 2014;12:198. Dosage error in article text. — View Citation

Nakai Y, Milgrom P, Mancl L, Coldwell SE, Domoto PK, Ramsay DS. Effectiveness of local anesthesia in pediatric dental practice. J Am Dent Assoc. 2000 Dec;131(12):1699-705. — View Citation

Segal MM, Douglas AF. Late sodium channel openings underlying epileptiform activity are preferentially diminished by the anticonvulsant phenytoin. J Neurophysiol. 1997 Jun;77(6):3021-34. — View Citation

Segal MM, Rogers GF, Needleman HL, Chapman CA. Hypokalemic sensory overstimulation. J Child Neurol. 2007 Dec;22(12):1408-10. doi: 10.1177/0883073807307095. — View Citation

Segal MM. We cannot say whether attention deficit hyperactivity disorder exists, but we can find its molecular mechanisms. Pediatr Neurol. 2014 Jul;51(1):15-6. doi: 10.1016/j.pediatrneurol.2014.04.014. Epub 2014 Apr 18. — View Citation

Teicher MH, Polcari A, Fourligas N, Vitaliano G, Navalta CP. Hyperactivity persists in male and female adults with ADHD and remains a highly discriminative feature of the disorder: a case-control study. BMC Psychiatry. 2012 Nov 7;12:190. doi: 10.1186/1471-244X-12-190. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Observational Study: Number of Participants With Lidocaine Ineffectiveness by Taste Test in Hard-to-treat ADHD Subjects will be asked to identify each taste and its intensity. on day of testing, approximately 30 minutes for clinic visit
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