Oxytocin and Arginine Vasopressin in Pain Relief
Stopped early
Conditions studied: Placebo Analgesia
In brief
Background: \- Oxytocin, a substance produced mostly in the brain, plays a role in influencing social interactions and reactions to stress, and may be related to pain. Arginine vasopressin, a hormone that regulates water, sugar, and salt in the blood, influences hostile behaviors and reactions to stress, and may also be related to pain. Researchers are interested in investigating both substances and their relationship to pain in healthy volunteers. Objectives: \- To evaluate the effects of oxytocin and arginine vasopressin on pain in healthy volunteers. Eligibility: \- Healthy volunteers between 18 and 55 years of age. Design: * This study involves two 2-hour testing sessions held 1 day apart. Each session includes the administration of oxytocin, arginine vasopressin, or placebo (a nonactive substance), or no drug. The drugs and the placebo will be given by a nasal spray. * At the first visit, participants will provide blood and saliva samples to measure hormone levels, and will be asked to fill out questionnaires about some psychological factors such as anxiety and empathy. Participants will then have an assessment of their sensitivity to pain, consisting of a brief electrical stimulation that lasts less than 1 second. After the pain assessment, participants will receive oxytocin, arginine vasopressin, placebo, or no drug at all, and will be monitored to provide baseline information. Participants will then have another pain sensitivity test and will complete the questionnaires again, and provide another saliva sample. * At the second visit, participants will provide another saliva sample; receive oxytocin, arginine vasopressin, placebo, or no drug at all; and have tests of pain sensitivity and a pain-relieving procedure. During the pain-relieving procedure, participants will receive brief, moderately painful electrical shocks on the back of the nondominant hand and a low-level electrical stimulation on the middle finger that counteracts or reduces the pain from the shocks. Participants will rate their pain perception at the end of each stimulation by using a visual scale ranging from 0 (no pain) to 10 (maximum imaginable pain). The experiment ends with a final saliva collection and completion of the psychological questionnaires.
Key facts
- Study ID
- NCT01328561
- Run by
- National Institute of Mental Health (NIMH)
- People needed
- 167
- Starts
- 2011-03-17
- Expected to finish
- 2015-03-04
- Last updated by the study team
- 2018-07-05
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may not qualify if…
- Any significant medical or neurological problems (e.g. cardiovascular illness, respiratory illness, neurologic illness, seizures, etc.)
- History of angioedema
- High blood pressure (above 140 mmHg) or symptomatic low blood pressure
- History of fainting
- A family history of mania, schizophrenia, or other psychoses (first-degree relatives only)
- A history of mania, schizophrenia, or other psychoses
- Any current Axis I psychiatric disorders (e.g. depression and anxiety)
- Lifetime alcohol/drug dependence
- Alcohol/drug abuse in the past year
- Current use of psychotropic medication
- Impaired hearing
- Pregnancy
- Breast-feeding
- Smokers (use of any form of nicotine during the last six months)
- Color-blindness (e.g. difficulty to distinguish between red and green colors)
- History of fainting and symptomatic hypotension will be reviewed by the clinicians responsible for the screening and study on a case-by-case basis.
- ADDITIONAL EXCLUSION CRITERIA FOR THE MRI AND MEG STUDIES
- Participants taking part in the MRI (Experiment 2) and MEG (Experiment 3) studies will also be excluded in case of:
- Metal slivers or shavings lodged in the tissues of the head or neck
- Surgical clips or shrapnel in or near the brain or blood vessels
- Any metallic objects in the eyes or central nervous system, and any form of implant wire or metal device that may concentrate radiofrequency fields
- Head trauma with loss of consciousness in the last year or any evidence of functional impairment due to and persisting after head trauma.
- Previously worked in metal fields or machines that may have left any metallic fragments in or near your eyes.
- Tattooed makeup (eyeliner, lip, etc) or general tattoos in a dangerous location on your body.
- Any non-organic implant or any other device such as: cardiac pacemaker, insulin infusion pump, implanted drug infusion device, cochlear, otologic, or ear implant, transdermal medication patch (Nitro), any metallic implants or objects, body piercing(s), bone/joint pin, screw, nail, plate, wire sutures or surgical staples, or shunt.
Where it is running
- National Institutes of Health Clinical Center, 9000 Rockville Pike — Bethesda, Maryland, United States
Full record on ClinicalTrials.gov
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