US2021101015A1PendingUtilityA1
Treatment of Thalamocortical Dysrhythmia
Est. expiryNov 25, 2032(~6.3 yrs left)· nominal 20-yr term from priority
Inventors:Steven Richard Devore Best
A61K 31/135A61P 29/00A61P 25/18A61P 25/00A61K 31/485A61P 25/30A61P 25/04A61P 43/00A61P 25/24A61P 25/02A61P 27/16A61P 25/16A61K 31/42A61M 19/00A61N 2/002A61N 2/02F04C 2270/0421A61N 1/36025A61M 2021/0055A61M 21/00A61N 1/36021A61N 2/006A61N 2/008A61M 2202/048A61K 45/06A61M 15/00
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Claims
Abstract
A method for treating conditions associated with thalamocortical dysrhythmia. The method includes applying transcranial low voltage electrical stimulation (TLVES) therapy or transcranial magnetic stimulation (TMS) therapy to a patient in need thereof, and administering to the patient a dissociative anesthetic during the TLVES therapy or the TMS therapy. A number of conditions including tinnitus, depression and pain can be treated with TLVES or TMS in combination with the dissociative anesthetic, such as an NMADR inhibitor, including ketamine.
Claims
exact text as granted — not AI-modified1 . A method for treating post-traumatic stress disorder (PTSD), the method comprising in combination,
administering intravenously, intramuscularly, orally, intranasally or by inhalation an N-methyl d-aspartate receptor (NMDAR) antagonist to a patient suffering from PTSD; applying, external to the skull, transcranial low voltage electric stimulation (TLVES) therapy or transcranial magnetic stimulation (TMS) therapy to the patient.
2 . The method of claim 1 , wherein the TLVES or TMS is further applied before or after the administration of the NMDAR antagonist.
3 . The method of claim 1 , wherein the NMDAR antagonist is ketamine, d-cycloserine, or dextromethorphan.
4 . The method of claim 3 , wherein ketamine is administered at a dose of about 50 mg to about 500 mg.
5 . The method of claim 3 , wherein ketamine is administered at a dose of about 0.5 mg/kg to about 5.0 mg/kg.
6 . The method of claim 1 , wherein the NMDAR antagonist is infused over a time period of between about 30 and 60 minutes.
7 . The method of claim 1 , wherein the TMS therapy comprises comprising 1-4 mAmps applied across brain tissue.
8 . A method for treating suicidality, the method comprising in combination, administering intravenously, intramuscularly, orally, intranasally or by inhalation an N-methyl d-aspartate receptor (NMDAR) antagonist to a patient suffering from suicidality;
applying, external to the skull, transcranial low voltage electric stimulation (TLVES) therapy or transcranial magnetic stimulation (TMS) therapy to the patient.
9 . The method of claim 8 , wherein the TLVES or TMS is further applied before or after the administration of the NMDAR antagonist.
10 . The method of claim 8 , wherein the NMDAR antagonist is ketamine, d-cycloserine, or dextromethorphan.
11 . The method of claim 10 , wherein ketamine is administered at a dose of about 50 mg to about 500 mg.
12 . The method of claim 10 , wherein ketamine is administered at a dose of about 0.5 mg/kg to about 5.0 mg/kg.
13 . The method of claim 8 , wherein the NMDAR antagonist is infused over a time period of between about 30 and 60 minutes.
14 . The method of claim 8 , wherein the TMS therapy comprises comprising 1-4 mAmps applied across brain tissue.
15 . A method for treating generalized anxiety, the method comprising in combination, administering intravenously, intramuscularly, orally, intranasally or by inhalation an N-methyl d-aspartate receptor (NMDAR) antagonist to a patient suffering from generalized anxiety;
applying, external to the skull, transcranial low voltage electric stimulation (TLVES) therapy or transcranial magnetic stimulation (TMS) therapy to the patient.
16 . The method of claim 15 , wherein the generalized anxiety includes panic attacks.
17 . The method of claim 15 , wherein the TLVES or TMS is further applied before or after the administration of the NMDAR antagonist.
18 . The method of claim 15 , wherein the NMDAR antagonist is ketamine, d-cycloserine, or dextromethorphan.
19 . The method of claim 18 , wherein ketamine is administered at a dose of about 50 mg to about 500 mg.
20 . The method of claim 18 , wherein ketamine is administered at a dose of about 0.5 mg/kg to about 5.0 mg/kg.
21 . The method of claim 15 , wherein the NMDAR antagonist is infused over a time period of between about 30 and 60 minutes.
22 . The method of claim 15 , wherein the TMS therapy comprises comprising 1-4 mAmps applied across brain tissue.Join the waitlist — get patent alerts
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