Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Aging
  • Epigenetics
  • Inflammatory Mediators
Type
Interventional
Phase
Early Phase 1
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Participants will be their own control, either right or left arm will be randomized to treatment or placebo.Masking: Double (Participant, Investigator)Masking Description: Randomization will be performed by the compounding pharmacy. Ointment dispensers will be color-coded for left and right arm for each subject.Primary Purpose: Treatment

Participation Requirements

Age
Between 65 years and 95 years
Gender
Both males and females

Description

Rapamycin 8% ointment will be applied topically to one of the participant's forearms and matching placebo to the opposite forearm daily for a total of 6 months. After consenting, screening and randomization of arms, the participants will be monitored at monthly visits until study completion.

Rapamycin 8% ointment will be applied topically to one of the participant's forearms and matching placebo to the opposite forearm daily for a total of 6 months. After consenting, screening and randomization of arms, the participants will be monitored at monthly visits until study completion.

Tracking Information

NCT #
NCT04608448
Collaborators
National Institute on Aging (NIA)
Investigators
Principal Investigator: Ellen Kraig, PhD University of Texas Health at San Antonio Principal Investigator: Dean L Kellogg, Jr., MD, PhD University of Texas Health at San Antonio