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Creatine Monohydrate Use for Preventing Altitude Induced Depression

Primary Purpose

Depression

Status
Withdrawn
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Creatine monohydrate
Placebo
Sponsored by
Mike O'Callaghan Military Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring depression

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

PATIENTS MUST BE ABLE TO GET CARE AT NELLIS AIR FORCE BASE (A MILITARY INSTALLATION) IN ORDER TO PARTICIPATE IN THIS STUDY

Inclusion Criteria:

  • Male and Female Active Duty members and DoD beneficiaries ages 18-65
  • Moved to CREECH AFB from an altitude of less than 2,000 feet within the last month

Exclusion Criteria:

  • Preexisting depression as noted in a review of their medical record or on their PHQ9 (score of 10 or greater)
  • Preexisting anxiety as noted in a review of their medical record or on their GAD 7 (score of 10 or greater)
  • Clinical or laboratory evidence of liver disease.
  • Serum creatinine >1.5
  • Existing kidney disease
  • Existing Type I or Type II Diabetes Mellitus
  • Taking creatine as a dietary supplement
  • Moved to CREECH AFB from an altitude of greater than 2000 feet
  • Pregnant, breast feeding, or trying to become pregnant

Sites / Locations

  • Mike O'Callaghan Military Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

creatine monohydrate

Placebo

Arm Description

Experimental will take by mouth 5 grams a day of creatine monohydrate powder. Subjects will be given a 30 day supply of the study powder. They will be reminded to take the powder as instructed.

Placebo will take by mouth 5 grams a day of placebo powder. Subjects will be given a 30 day supply of the study powder. They will be reminded to take the powder as instructed.

Outcomes

Primary Outcome Measures

Patient Health Questionnaire-9 (PHQ-9)
Questionnaire
Generalized Anxiety Disorder 7 (GAD-7)
Questionnaire

Secondary Outcome Measures

Full Information

First Posted
February 8, 2018
Last Updated
January 7, 2019
Sponsor
Mike O'Callaghan Military Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03433651
Brief Title
Creatine Monohydrate Use for Preventing Altitude Induced Depression
Official Title
Creatine Monohydrate Use for Preventing Altitude Induced Depression
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Withdrawn
Why Stopped
Unable to locate grant funding.
Study Start Date
January 1, 2019 (Actual)
Primary Completion Date
January 7, 2019 (Actual)
Study Completion Date
January 7, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mike O'Callaghan Military Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study involves the use of an investigational drug called Creatine Monohydrate. This means that the drug has not yet been approved by the Food & Drug Administration (FDA) for treatment of altitude-induced depression. However, the FDA has not objected to its use to study its safety and effectiveness for preventing altitude-induced depression. This study will help find out what effects, good and/or bad, Creatine Monohydrate has on treating symptoms for altitude-induced depression. Creatine Monohydrate is believed to have an effect on improving symptoms of depression. The safety of Creatine Monohydrate in humans has been tested in prior research studies; however, some side effects may not yet be known.
Detailed Description
Subjects will be in this research study if they moved to Creech AFB from an elevation of less than 2.000 feet within the last month. The purpose of this study is to see if creatine monohydrate is effective in preventing altitude-induced depression. This study will enroll approximately 75 subjects. This study involves the use of an investigational drug called Creatine Monohydrate. This means that the drug has not yet been approved by the Food & Drug Administration (FDA) for treatment of altitude-induced depression. However, the FDA has not objected to its use to study its safety and effectiveness for preventing altitude-induced depression. This study will help find out what effects, good and/or bad, Creatine Monohydrate has on treating symptoms for altitude-induced depression. Creatine Monohydrate is believed to have an effect on improving symptoms of depression. The safety of Creatine Monohydrate in humans has been tested in prior research studies; however, some side effects may not yet be known. Creatine Monohydrate is a dietary supplement that is believed to aid in the building of muscle mass. The placebo being used in this study is Maltodextrin (a sugar). Maltodextrin is an FDA approved food additive made from a highly processed starch product typically made from corn.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression
Keywords
depression

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Masking Description
Subjects will be randomized using a random number generator to receive either creatine monohydrate or a placebo for 90 days. Both subjects and investigators will be blinded to the study group assignments
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
creatine monohydrate
Arm Type
Experimental
Arm Description
Experimental will take by mouth 5 grams a day of creatine monohydrate powder. Subjects will be given a 30 day supply of the study powder. They will be reminded to take the powder as instructed.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo will take by mouth 5 grams a day of placebo powder. Subjects will be given a 30 day supply of the study powder. They will be reminded to take the powder as instructed.
Intervention Type
Drug
Intervention Name(s)
Creatine monohydrate
Other Intervention Name(s)
creapure
Intervention Description
Subjects will take by mouth 5 grams a day of creatine monohydrate powder.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
maltodextrin
Intervention Description
Subjects will take by mouth 5 grams a day of placebo powder.
Primary Outcome Measure Information:
Title
Patient Health Questionnaire-9 (PHQ-9)
Description
Questionnaire
Time Frame
5 repeated measurements over the 120-day course of the study
Title
Generalized Anxiety Disorder 7 (GAD-7)
Description
Questionnaire
Time Frame
5 repeated measurements over the 120-day course of the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
PATIENTS MUST BE ABLE TO GET CARE AT NELLIS AIR FORCE BASE (A MILITARY INSTALLATION) IN ORDER TO PARTICIPATE IN THIS STUDY Inclusion Criteria: Male and Female Active Duty members and DoD beneficiaries ages 18-65 Moved to CREECH AFB from an altitude of less than 2,000 feet within the last month Exclusion Criteria: Preexisting depression as noted in a review of their medical record or on their PHQ9 (score of 10 or greater) Preexisting anxiety as noted in a review of their medical record or on their GAD 7 (score of 10 or greater) Clinical or laboratory evidence of liver disease. Serum creatinine >1.5 Existing kidney disease Existing Type I or Type II Diabetes Mellitus Taking creatine as a dietary supplement Moved to CREECH AFB from an altitude of greater than 2000 feet Pregnant, breast feeding, or trying to become pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lee Church, MD
Organizational Affiliation
Mike O'Callaghan Military Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mike O'Callaghan Military Medical Center
City
Las Vegas
State/Province
Nevada
ZIP/Postal Code
89191
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
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Creatine Monohydrate Use for Preventing Altitude Induced Depression

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