Actively Recruiting
Effects Of Intravenous Oxytocin On Peripheral Sensory Afferents Using Microneurography
Led by Wake Forest University Health Sciences · Updated on 2026-02-13
60
Participants Needed
1
Research Sites
84 weeks
Total Duration
On this page
Sponsors
W
Wake Forest University Health Sciences
Lead Sponsor
N
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if oxytocin reduces pain in a small area of skin after pulses of non-burning heat by changing how nerves in the heated area react to pressing a thin, bendable plastic bristle and a thick, non-bending plastic bristle in adult, healthy participants. The man questions it aims to answer are: Does oxytocin increase the number of times a fiber which normally responds only to the thin bristle fires (sends a signal) after the heat pulses. Does oxytocin raise the number of times a fiber which normally responds only to the thick bristle fires (sends a signal) after the heat pulses. Researchers will compare oxytocin to a placebo (a look-alike substance that contains no drug) to see if oxytocin ABC works to change how nerves react to light touch and painful pressing in an area of sensitized skin. Participants will: Receive an intravenous injection of oxytocin or placebo on one occasion On the same day, a needle will be put near nerve fibers to record their firing before and after a few cycles of short heating of the skin.
CONDITIONS
Official Title
Effects Of Intravenous Oxytocin On Peripheral Sensory Afferents Using Microneurography
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 65 years
- In good health based on medical, psychiatric, and lab assessments
- Female participants of child-bearing potential must use highly effective birth control or abstain for at least one full cycle before treatment
- Normal blood pressure (90-140 mmHg systolic; 50-90 mmHg diastolic) and resting heart rate (45-100 bpm) without medication
- Proficient in Swedish or English
You will not qualify if you...
- Allergy or significant reaction to oxytocin or placebo ingredients
- Any medical or surgical condition that increases risk or affects study compliance or data quality
- Women who are pregnant, nursing, or have been pregnant within 2 years
- Body mass index (BMI) over 30
- Having neuropathy, chronic pain, diabetes, or daily use of benzodiazepines or pain medications
- History or current ventricular tachycardia, atrial fibrillation, or prolonged QT interval
- History or risk of hyponatremia or taking specific medications including diuretics, lithium, antidepressants, or recreational drugs
- Known latex allergy
- Substance use disorders or other psychiatric disorders
- High risk of fainting episodes
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Trial Site Locations
Total: 1 location
1
Linköping University
Linköping, Sweden, 58183
Actively Recruiting
Research Team
H
Hakan Olausson, MD, PhD
CONTACT
S
Saad Nagi, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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