Clinical Trials Logo
  1. Home
  2. Patient Activation
  3. NCT05689697

Induced Physiological Ketosis in Asthenia and\or Decreased Tolerance to Physical and\or Mental Exertion

Patient Activation Clinical Trial

Official title:
Efficacy of Physiological Ketosis Induced by Liquid Technology Formula PanTrek in Asthenia and\or Decreased Tolerance to Physical and\or Mental Exertion (Double-blind, Placebo-controlled Study)

Clinical Trial Summary

The purpose of this study is evaluating of efficacy of innovative dietary strategy -stimulation of physiological ketosis with Liquid Technology Formula PanTrek, in patients with asthenia and or decreased tolerance to physical and\or mental exertion. PanTrek is a liquid formula of potassium and magnesium salts of beta-oxibutiric acid, ginsenosides and rosmarinic acid.

Clinical Trial Description

It will be double-blind, placebo-controlled study in 88 patients of both sex, aged from 18 to 65. Patients will be randomly assigned to one of two groups: placebo or IP group in 1:1 proportion. Study instruments: D-Fis, MoCA, TMT, VAS, assessment of blood keton concentration before and after first and last administration per os of 25 ml of placebo or PanTrek. PanTrek will be served in ampuls, 25 ml per ampule. The duration of the study will be 15 days of treatment and 15 days of follow-up observation. Patients will be assessed at screening/baseline, after 15 days and after 30 days. The dose regimen: the shot of PanTrek, 25 ml, will be administered per os, twice per day, in the morning and in the evening, per se or deluted in 100 ml of water one hour before or after meal. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05689697
Study type Interventional
Source Ketonic Pharm LLC
Contact Denis Burminskiy, MD, PhD
Phone +79262344633
Email desbur@gmail.com
Status Not yet recruiting
Phase N/A
Start date January 9, 2023
Completion date August 15, 2023
View Details
See also
  Status Clinical Trial Phase
Completed NCT05071248 - Evaluation of the Effect of Robot-assisted Early Mobilization - Project MobiStaR N/A
Recruiting NCT03828318 - Impact of a Patient-Centered Program for Low Anterior Resection Syndrome A Multicenter Randomized Controlled Trial N/A
Completed NCT04160650 - Educational Nursing Intervention Among Patients With Colorectal Cancer During Chemotherapy N/A
Recruiting NCT05658393 - Web-based Mobile Health Application for Patients With Liver Cirrhosis (ReLiver-N App) N/A
Active, not recruiting NCT04988880 - Territorial Implementation and Evaluation of a Multiple Sclerosis Expert Patient Program N/A
Recruiting NCT05880368 - Partnership in Resilience for Medication Safety (PROMIS) N/A
Recruiting NCT05989477 - At-home Breast Oncology Care Delivered With E-health Solutions N/A
Completed NCT06236529 - Self-Management of Chronic Low Back Pain: Targeting Patient Activation N/A
Not yet recruiting NCT05900687 - Developing and Testing Mobile Health Question Prompt List in Gastroesophageal Reflux Disease N/A
Not yet recruiting NCT05902156 - Electronic Patient Decision Support System for Patients With Type 2 Diabetes (DiaPaDeSS) N/A
Completed NCT03385512 - OPEN & ASK: Improving Patient-Centered Communication in Primary Care N/A
Completed NCT03334188 - Electronic Health Record-leveraged, Patient-centered, Intensification of Chronic Care for HF N/A
Completed NCT04224220 - Effectiveness of Nurse-based Care Coordination on Readmissions Among Primary Care Patients: a Stepped Wedge Cluster Randomized Trial N/A
Recruiting NCT05263310 - Prepare for Your Diabetes Care N/A