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Search / Trial NCT06329037

The Effects of Oral Vasopressin on Attention Control: An Eye-tracking Study

Launched by UNIVERSITY OF ELECTRONIC SCIENCE AND TECHNOLOGY OF CHINA · Mar 15, 2024

Trial Information

Current as of August 19, 2025

Recruiting

Keywords

Eye Tracking Vasopressin

ClinConnect Summary

This clinical trial is investigating how a medication called vasopressin, taken by mouth, affects attention control in healthy individuals. Specifically, the study aims to see how this medication influences our ability to focus on important social and emotional cues, using a method that tracks eye movements. The researchers are looking for healthy volunteers aged between 18 and 65 who can read and understand the study details and give their consent to participate.

If you choose to participate, you will be part of a randomized study, meaning you might receive either the vasopressin or a placebo (a sugar pill with no active medication) without knowing which one you have. To be eligible, you should not have any history of serious medical conditions, like heart or liver diseases, and must not be pregnant or breastfeeding. This trial is currently recruiting participants, and it provides a chance to contribute to research that may help us understand how our brains process attention.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Healthy subjects who volunteer to participate and are able to fully understand and agree with this study by written informed consent.
  • Normal or corrected-normal version
  • Exclusion Criteria:
  • History of neuropsychiatric diseases.
  • History of cardiac disease, including arrhythmias, aortic stenosis, or congestive heart failure; history of syncope or unexplained loss of consciousness.
  • History of hepatic diseases, including cholestasis, biliary obstructive disease, or severe liver dysfunction.
  • History of renal diseases, including renal stones or renal failure.
  • History of hyponatremia(Serum sodium \<135mmol/L) or hyperkalemia (Serum potassium\>5.5mmol/L); history of diabetes mellitus or diabetes insipidus
  • Known hypersensitivity or allergic reaction to any medication or hormone; strong allergic reaction to food.
  • Infections such as COVID-19 or influenza, or unexplained fever.
  • Subjects with hypertension (BP ≥130/80mmHg) or hypotension (BP ≤ 90/60mmHg).
  • History of alcohol or drug abuse; smoker (≥ 10 cigarettes or ≥ 3 cigars or ≥ 3 pipes/day); smoker using e-cigarettes.
  • Blood donation (≤ 1 month prior to administration).
  • Take oral contraceptives or receive hormonal medications in the three months prior to the experiment.
  • Pregnant or breastfeeding.

About University Of Electronic Science And Technology Of China

The University of Electronic Science and Technology of China (UESTC) is a leading institution renowned for its research and innovation in electronics and information technology. Established with a commitment to advancing scientific knowledge and fostering technological development, UESTC plays a pivotal role in clinical research, particularly in the integration of electronic technologies with healthcare. The university's robust academic framework, combined with its focus on interdisciplinary collaboration, enables the design and execution of clinical trials that aim to enhance medical practices and improve patient outcomes. Through its dedication to excellence and innovation, UESTC contributes significantly to the advancement of healthcare solutions on both a national and global scale.

Locations

Chengdu, Sichuan, China

Patients applied

0 patients applied

Trial Officials

Benjamin Becker, Dr

Principal Investigator

University of Electronic Science and Technology of China

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported