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Multicenter exploratory clinical study for investigating pulse wave characteristics of infertility patients

Clinical study on pulse wave data collection of Infertility patients : A multicenter exploratory clinical trial?

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0002508
Enrollment
80
Registered
2017-10-27
Start date
2016-10-12
Completion date
Unknown
Last updated
2020-08-18

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) Woman aged 20 to 44 years 2) Diagnosed with unexplained infertility from obstetrics and gynecology specialists 3) Woman who has intercourse with reasonable frequency at least twice or more per week except during menstrual period

Exclusion criteria

Exclusion criteria: 1) Taking or planning of taking medication for infertility like hormonal drugs, herbal medicine 2) Planning of artificial insemination or in vitro fertilization(IVF) 3) Irregular menstrual cycle more than 40 days or less than 21 days 4) Male factor infertility 5) Ovulation related infertility like polycystic ovarian syndrome, Thyroid Disease, Hyperprolactinemia 6) Tubal and peritoneal factor, cervical factor related infertility like endometriosis, pelvic inflammatory disease, uterine fibroids, uterine adenomyosis 7) IVF 4 times over the past 8) Patients with any neuropsychiatric condition. 9) The other condition, which makes the patient unsuitable for inclusion in the opinion of investigator (uncontrolled hypertension, diabetes mellitus , endocrine disease, acute, chronic hepatitis/cirrhosis, severe hyperlipidemia, severe heart disease, lung disease, Tbc, other infectious disease) 10) Past history of cancer within five years 11) Individuals who are judged unable to fill out the forms related to research performance 12) History of adverse reaction to pulse tonometric device (PTD) 13) Congenital vascular anomalies or history of wrist fracture 14) Anyone considered inappropriate for participating in this trial by the clinical trial conductors

Design outcomes

Primary

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

Secondary

MeasureTime frame
Pulse tonometric devices' parameter (pulse depth index);Pulse tonometric devices' parameter (pulse volume index);Pulse tonometric devices' parameter (hear rate)

Countries

Korea, Republic of

Contacts

Public ContactDong Kim

Dongguk University Ilsan Oriental Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026