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Exploratory observational study on the pulse waveform of dysmenorrhea patients and healthy subjects according to their menstrual period

Exploratory observational study on the pulse waveform of dysmenorrhea patients and healthy subjects according to their menstrual period

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0001604
Enrollment
48
Registered
2015-08-27
Start date
2015-08-10
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Korea Institute of Oriental Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1) Female aged 20 to 30 years 2) Women with a period cycle of 28 ± 3 days during last 3 months 3) Women who have menstrual pain (dysmenorrhea) over 4 degrees by Visual Analogue Scale (VAS) 4) Woman who can communicate with clinical study researcher and fill out a questionnaires 5) Woman who have a voluntary agreement and participation in this clinical study 6) Given written informed consent form.

Exclusion criteria

Exclusion criteria: 1) Women with secondary dysmenorrhea caused by uterine myoma, endometriosis, ophorociptosis and infection of genitals confirmed by ultrasound exam 2) Women who have medical operations and procedures 3) who have major neuro-psychiatric disorder or have history of major neuro-psychiatric disorder, and women who are taking anti-depressant, anti-serotonin barbiturate, psychotropic drugs with 3 months 4) Women who have major medical disease or have history of major medical disease (hypertension, diabetes, hyperlipidemia, gastritis, enteritis, gastro-esophageal reflux disease, Crohn’s disease etc.) 5) Women who have an drastic diet within 1 week 6) Women who are pregnant, as determined by a urine pregnancy test 7) History of adverse reaction to pulse tonometric device 8) Women who have congenital vascular anomaly and experience fracture of the wrist 9) Received clinical study within one month prior to enrollment 10) Any other condition likely in the judgment of the investigator that make the participants unable to complete, or is unsuitable for the study.

Design outcomes

Primary

MeasureTime frame
Pulse tonometric devices' parameter (pulse pressure index)

Secondary

MeasureTime frame
InBody 720s' parameters (intercellular water, extracellular water, protein, mineral, body fat mass, extracellular water/total body water ratio);Total score of Measurement of Menstrual Pain (MMP);Total score of Self-rating Anxiety Scale (SAS);Toral score of Self-rating Depression Scale (SDS);Total score of Cold and Heat Pattern Questionnaire (CHPQ);Total score of Phlegm Pattern Questionnaire (PPQ);Total score of Blood Stasis Pattern Questionnaire (BSPQ);Total score of Food Accumulation Pattern Questionnaire (FAPQ);Total score of Seven Emotions Pattern Questionnaire (SEPQ);Total score of Fatigue Pattern Questionnaire (FPQ);Pulse tonometric devices' parameter (pulse rate);Pulse tonometric devices' parameters (pulse depth index);Pulse tonometric devices' parameters (pulse volume index);Tongue image

Countries

Korea, Republic of

Contacts

Public ContactHyunho Kim

Kyung Hee University

mechante@hanmail.net+82-2-958-9242

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 27, 2026