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Oxtocin administration experiment(Menstrual cycle analysis)

Not Applicable
Recruiting
Conditions
Healthy Females
Registration Number
JPRN-jRCTs051210118
Lead Sponsor
Satoshi Nakagawa
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
250
Inclusion Criteria

For those who meet all of the following criteria.
(1) Premenopausal healthy women
(2) Age: 18<= and <45 at the point of informed consent
(3) No serious disease under medical treatment
A healthy woman is defined as a woman who does not have any abnormality that meets the exclusi on criteria and who has not been found to have any abnormality that requires treatment in a school or workplace examination conducteds after fiscal 2021.To determine the eligibility criteria,it is necessary to submit the results of a school or workplace medical checkup, and following items are confirmed by the
docors.
Check items:
(1) The absence of significant edema
(2) Systolic blood pressure < 140 mgHg and diastolic blood pressure < 90 mmHg
(3) No possibility of pregnant
(4) No ECG abnormalities that require awareness or treatment of arrhythmia

Exclusion Criteria

Those who fall under any of the following criteria will be excluded from the research subjects of this clinical research.
(1) Pregnant and breastfeeding women(Including within 1 year after delivery)
(2) History of tretment with oxytocin
(3) History of head injury with impaired consciousness for more than 5 minutes
(4) Drug dependence or alcohol dependence or their previous history
(5) History of water intoxication with consciousness or seizures
(6) Polydipsia (remarkably daily heavy drinking more than 2.5L per day)
(7) Those who are aware of arrhythmia or have abnormal ECG
(8) Those who taking pill
(9) Any other interested person
(10)When the research investigator determines inappropriate case for the other reasons.
(e.g., when drug absorption through the nasal mucosa is considered to be difficult due to previous nasal surgery)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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