RECRUITING

Magnesium and Riboflavin Treatment for Post-Concussion Headache

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This clinical trial will try to determine if the supplements magnesium and riboflavin will reduce the pain and duration of headaches in persons diagnosed with a concussion. The participant will be randomized to either active magnesium and riboflavin capsules or placebo (inert) capsules. The capsules will be taken once a day for 14 days. The participant will also complete a short diary form for the 14 days and will have 3 follow up visits either by telephone or in person.

Official Title

Magnesium and Riboflavin Treatment for Post-Concussion Headache

Quick Facts

Study Start:2020-02-10
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06260072

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 40 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Seen at University of Virginia Student Health and Wellness Center or Emergency Department for Initial Visit for Concussion;
  2. * Less than 3 days have elapsed since their injury;
  3. * Able to swallow capsules
  1. * Concussion complicated by cranial bleed, skull fracture, additional severe injury;
  2. * Kidney disfunction or failure;
  3. * Significant gastro-intestinal dysfunction;
  4. * Varsity Athlete;
  5. * Two or more previous concussions;
  6. * Women who are pregnant or breast feeding;
  7. * Taking tetracycline, fluoroquinolone, iron digoxin, chlorpromazine or penicillamine

Contacts and Locations

Study Contact

Stephanie Hartman, MD
CONTACT
434-924-5362
slm8nh@virginia.edu
Karen Ahern, BSN MBA
CONTACT
4340924-1549
kaa7p@virginia.edu

Principal Investigator

Stephanie Hartman, MD
PRINCIPAL_INVESTIGATOR
UVA Student Health and Wellness

Study Locations (Sites)

University of Virginia Student Health and Wellness Center
Charlottesville, Virginia, 22903
United States

Collaborators and Investigators

Sponsor: University of Virginia

  • Stephanie Hartman, MD, PRINCIPAL_INVESTIGATOR, UVA Student Health and Wellness

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-02-10
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2020-02-10
Study Completion Date2024-12-31

Terms related to this study

Keywords Provided by Researchers

  • Concussion; Headache

Additional Relevant MeSH Terms

  • Concussion, Intermediate