Clinical trial

Evaluating Potential Benefits of Intranasal Oxytocin on Undersea Operator Training and Performance: Cold Water Task Performance and Recovery

Name
IRB-2020-0002
Description
Naval Special Warfare (NSW) operators are exposed to a variety of extreme environmental conditions and intense physical demands. In addition to breathing high pressure gases at depth, prolonged cold water immersion and inadequate recovery from sustained physical exertion negatively impact individual and team performance. Biotechnologies that could mitigate the effects of cold as well as support physical recovery represent a significant unmet need for the NSW operational community. Oxytocin (OT) has a wide range of actions both locally in the brain and peripherally in the body including skeletal muscle. These peripheral effects can be mediated by classic ligand-receptor activation given the abundant expression of the oxytocin receptor in peripheral tissues, along with local expression of OT in peripheral tissues where it is likely to act in an autocrine manner. Exogenous OT via intranasal administration is FDA Investigational New Drug (IND)-approved and has been demonstrated as an easy and safe method to increase circulating OT concentrations that may augment actions on peripheral tissues.
Trial arms
Trial start
2022-05-20
Estimated PCD
2022-07-29
Trial end
2022-07-29
Status
Completed
Phase
Early phase I
Treatment
Oxytocin nasal spray
Intranasal treatment with oxytocin via nasal spray (48 IU per dose)
Arms:
Oxytocin Nasal Spray
Other names:
Oxytocin
Placebo nasal spray
Intranasal treatment with placebo via nasal spray
Arms:
Placebo Nasal Spray
Other names:
Placebo
Size
17
Primary endpoint
Cognitive performance assessment score change (code substitution)
Within 3 hours post-treatment
Cognitive performance assessment score change (code substitution)
Within 3 hours post-treatment
Cognitive performance assessment score change (reaction time)
Within 3 hours post-treatment
Cognitive performance assessment score change (reaction time)
Within 3 hours post-treatment
Oculometric assessment score change (saccades)
Within 3 hours post-treatment
Oculometric assessment score change (blink rate)
Within 3 hours post-treatment
Oculometric assessment score change (blink duration)
Within 3 hours post-treatment
Eligibility criteria
Inclusion Criteria: * Recreationally skilled swimmers Exclusion Criteria: * Smoking/vaping, a history of psychiatric disorders, safety requirements related to the oxytocin administration \[hypersensitivity to oxytocin or vasopressin, history of hyponatremia, syndrome of inappropriate antidiuretic hormone secretion, or psychogenic polydipsia, on vasoconstrictors such as desmopressin, pseudoephedrine, or antidiuretic medication, or anti-inflammatory drugs, or muscle relaxants, low sodium and high osmolality levels, excessive smoking, excessive drinking, and significant nasal pathology.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'CROSSOVER', 'interventionModelDescription': 'Double-blind, placebo-controlled, randomized crossover design', 'primaryPurpose': 'PREVENTION', 'maskingInfo': {'masking': 'QUADRUPLE', 'maskingDescription': 'All will remain blinded until completion of human subjects data collection except the research pharmacist providing intranasal oxytocin or placebo.', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 17, 'type': 'ACTUAL'}}
Updated at
2024-02-22

1 organization

2 products

1 indication

Product
Oxytocin
Indication
Hypothermia