Recruiting

Observational Study

Sponsor:

University of Delaware

Code:

NCT06860724

Conditions

Major Depressive Disorder

Eligibility Criteria

Sex: All

Age: 18 - 55

Healthy Volunteers: Accepted

Interventions

NG-nitro-L-arginine methyl ester (L-NAME)

Study Details

Brief summary:

The objective of this proposal is to determine whether heightened negative affective responsivity (NA-R) to daily stressors is related to blunted nitric oxide (NO)-mediated endothelium-dependent dilation (EDD) in working age adults and the extent to which this association is impacted by major depressive disorder (MDD).

Conditions

Major Depressive Disorder

Study ID

NCT06860724

Start date

Jan 6, 2025

Status verified date

Feb, 2025

Completion date

Dec 1, 2031

Anticipated

Primary completion date

Dec 30, 2030

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 55

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Males and females aged 18-55 yrs
  • Non-depressed health adults (HA) will have no evidence of current or lifetime history of major psychiatric illness, assessed by the MINI and self-report and confirmed by a Licensed Clinical Psychologist
  • Adults with major depressive disorder (MDD) must meet the DSM-5 criteria for MDD and be currently symptomatic, assessed by the MINI and confirmed by a Licensed Clinical Psychologist; participants with co-morbid anxiety, stress, and trauma-related disorders will be included
  • Absence of unstable or chronic clinical disease, including cardiovascular, metabolic, renal, hepatic, autonomic, autoimmune, or dermatological disease, as determined by medical history, physical examination, blood chemistries, and 12-lead resting electrocardiogram; however, to ensure a more generalizable sample, adults with elevated systolic BP (<130mmHg), direct low-density lipoprotein (<160mg/dl), and glucose (HbA1c <5.7%) will be included
  • Participants must have a level of understanding of the English language sufficient to provide informed consent and to agree to all tests and procedures, as well as the capacity and willingness to attend all study related visits and to comply with the study protocol

Exclusion Criteria:

Subjects will be excluded at the discretion of the PI/collaborating clinicians or for any of the following reasons:

  • <18 or >55 yrs
  • Lifetime or current co-morbid neuropsychiatric disease (bipolar disorder, psychotic disorders, schizophrenia, eating disorders, obsessive-compulsive disorder, alcohol or substance use disorders)
  • Serious and imminent active suicidal/homicidal ideation with intent, plans, or behaviors, determined by the Licensed Clinical Psychologist or other clinical study team staff
  • Diagnosed chronic clinical disease, including cardiovascular, metabolic, renal, hepatic, autonomic, autoimmune, or dermatological disease, as determined by medical history, physical examination (resting systolic BP ≥130mmHg, body mass index ≥35 kg/m2), clinically significant abnormal blood chemistries (direct low-density lipoprotein ≥160mg/dl, HbA1c≥5.7%), and clinically significant abnormal 12-lead resting ECG
  • Current or recent use (within last 8 wks) of medications that alter cardiovascular function or psychoactive or psychopharmacological drugs \[including (but not limited to) antidepressants, antipsychotics, benzodiazepines, mood stabilizers, sedatives/hypnotics, dopaminergic agents, stimulants, buspirone, and triptans\]
  • Tobacco use (including electronic cigarettes)
  • Females who are pregnant, breastfeeding, or planning to become pregnant; female subjects of child-bearing age must have a negative urine pregnancy test on the day of all experimental visits
  • Current or past use of hormone replacement therapy
  • Allergy to study drugs or pharmacological agents

Study Design

Enrollment

18 participants

Anticipated

Allocation

Non randomized

Intervention Model

Parallel Assignment

Primary purpose

Basic Science

Interventions and Outcome Measures

Arms

active comparator: healthy adults

non-depressed healthy adults

experimental: adults with major depressive disorder

adults with major depressive disorder (unmedicated)

Interventions

NG-nitro-L-arginine methyl ester (L-NAME)

Acute local perfusion of L-NAME (15 mM) directly to the microvasculature will be used to inhibit NO synthase.

Primary outcome measure

  • Nitric oxide (NO)-mediated endothelium-dependent dilation (EDD) [ Time Frame: immediately before and after the 14-day testing cycle ]
  • Negative affective responsivity (NA-R) to daily stressors [ Time Frame: immediately after the 14-day testing cycle ]

Central Contacts and Locations

Central contacts

Locations

University of Delaware

Recruiting

Newark, Delaware, United States, 19713

Contacts

More Information

Sponsor

University of Delaware

Last update posted

Sep 17, 2025

Last verified

Feb, 2025

Keywords

  • stress
  • affect
  • endothelial function

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Delaware on 2025-09-17.