Viewing Study NCT06575972



Ignite Creation Date: 2024-10-26 @ 3:39 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06575972
Status: COMPLETED
Last Update Posted: None
First Post: 2024-08-23

Brief Title: A Clinical Study to Assess the Effects of JoyRise Recovery Powder on Mitigating Alcohol Aftereffects
Sponsor: None
Organization: None

Study Overview

Official Title: A Clinical Study to Assess the Effects of JoyRise Recovery Powder on Mitigating Alcohol Aftereffects
Status: COMPLETED
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study assesses the effectiveness of JoyRise Recovery Powder in reducing alcohol aftereffects cognitive impairment and anxiousness among participants aged 35-54 who consume alcohol Participants will be randomly assigned to either the JoyRise group or a placebo group The study will measure hangover symptoms cognitive function and overall well-being through a series of questionnaires and cognitive tests at baseline 30 minutes after product consumption and 4 hours later
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None