Clinical Trials Directory

Trials / Terminated

TerminatedNCT02189915

Open-Label Creatine Study for Female Meth Users

Open-Label Creatine Monohydrate Supplementation in Depressed Female Methamphetamine Users

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
14 (actual)
Sponsor
Perry Renshaw · Academic / Other
Sex
Female
Age
13 Years – 55 Years
Healthy volunteers
Accepted

Summary

Study Purposes and Objectives: The objectives should be stated in such a way that the reader can determine the appropriateness of the study design. If appropriate, state the specific hypotheses being tested and/or study aims. Use lay language. Methamphetamine use is of great concern in the state of Utah because it's the primary drug of threat in the state, and is the primary drug of choice among females between the ages of 18 and 24. The primary hypothesis of the study is that eight weeks of oral creatine supplementation will result in improvements in depression rating scores in female MA users. Secondary hypotheses include the following: 1) creatine supplementation will result in a decrease in the number of positive MA screens; 2) NAA and Cr concentrations will increase after eight weeks of oral creatine supplementation; and 3) PCr/β-NTP levels in the frontal lobe using 31P MRS will increase after eight weeks of creatine monohydrate oral supplementation.

Conditions

Interventions

TypeNameDescription
DRUGCreatine monohydrate

Timeline

Start date
2012-01-01
Primary completion
2015-10-01
Completion
2015-10-01
First posted
2014-07-15
Last updated
2016-05-20
Results posted
2016-05-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02189915. Inclusion in this directory is not an endorsement.