drugset / Trial / NCT06560944

Oral Contraceptive Consumption Timing and Cognition and Metabolism

NCT06560944

Completed 16 enrolled University of Lincoln
RandomizedCrossoverDouble-blindOther

Summary

The aim of this randomised-controlled trial is to examine whether the timing of oral contraceptive administration affects cognitive function, substrate metabolism and exercise performance. Participants will attend the laboratory for a familiarisation session, followed by two main trials in which cognition and exercise metabolism and performance are measured. In one trial they will be given their oral contraceptive 60 minutes before testing begins, in the other they will be given a placebo. Following testing (\~60 minutes), participants will consume the alternative pill.

Timeline

Start
2020-01-17
Primary completion
2024-01-20
Completion
2024-01-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Levonorgestrel Small molecule 150 mg Oral
Subject ethinyl estradiol Small molecule 30 ug Oral

Indications

No indication recorded.