drugset / Trial / NCT06460948

Identifying Oxytocin Deficiency in Adults With Pituitary Disease

NCT06460948 ↗

Phase 0 Completed 28 enrolled Elizabeth Austen Lawson
Non-randomizedParallel-groupOpen-labelDiagnostic

Summary

This is an open-label, pilot study, to characterize oxytocin response to a single dose of oral Estrogen-progestin in patients with arginine-vasopressin deficiency compared to healthy controls. The association between oxytocin levels and measures of psychopathology (i.e., anxiety and depression) and quality of life across groups will be examined. We hypothesize that: 1. Salivary and blood oxytocin response to Estrogen-progestin will be lower in arginine-vasopressin deficiency compared to healthy control. 2. Lower salivary and blood oxytocin levels will be associated with more severe symptoms of anxiety, depression, and social emotional difficulties as well as lower quality of life.

Timeline

Start
2024-11-13
Primary completion
2026-03-17
Completion
2026-03-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Norethindrone Acetate-Ethinyl Estradiol Unknown — —