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

Not Applicable

Completed

• Conditions: Diseases of The genitoruinary system

• Registration Number: KCT0002508
• Lead Sponsor: Korea Institute of Oriental Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 18 August 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 80

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

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

Study & Design

• Study Type: Observational Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pulse tonometric devices' parameter (pulse pressure index)

Secondary Outcome Measures

Name	Time	Method
Pulse tonometric devices' parameter (pulse depth index);Pulse tonometric devices' parameter (pulse volume index);Pulse tonometric devices' parameter (hear rate)