Identification and Clinical Relevance of an Oxytocin Deficient State (CRH Study)

PHASE4CompletedINTERVENTIONAL
Enrollment

52

Participants

Timeline

Start Date

July 6, 2021

Primary Completion Date

April 30, 2023

Study Completion Date

May 1, 2023

Conditions
HypopituitarismCentral Diabetes InsipidusPanhypopituitarismPsychological DisorderSocial IsolationHypothalamic DiseasesPituitary DiseasesOxytocin Deficiency
Interventions
DRUG

Experimental: CRH administration

CRH at 1.0 µg/kg/body weight will be injected intravenously as a bolus over 30 seconds and samples will be collected over 2 hours (15 (T15), 30 (T30), 45 (T45), 60 (T60'), 90 (T90) and 120 (T120) minutes) after CRH:placebo administration to assess OT secretory patterns

DRUG

Control: Placebo administration

Sodium Chloride 0.9% will be administered intravenously as a bolus over 30 seconds at equivalent volume than CRH administration (1.0 µg/kg/body weight)

Trial Locations (1)

08041

Hospital de la Santa Creu i Sant Pau, Barcelona

All Listed Sponsors
collaborator

Instituto de Salud Carlos III

OTHER_GOV

lead

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

OTHER