Tokyo, April 9 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061198) titled 'Development and usability study of a decision-making aid for men considering treatment with assisted reproductive technologies' on April 8.
Study Type:
Observational
Primary Sponsor:
Institute - Tokyo Healthcare University
Condition:
Condition - infertility
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - This study will examine the content and face validity of a prototype decision-making aid for men undergoing infertility treatment who are considering stepping up to testicular sperm extraction (TESE), an assisted reproductive technology. The aid will be tested with healthcare professionals and individuals with experience of infertility treatment.
Basic objectives2 - Others
Eligibility:
Age-lower limit - Not applicable
Age-upper limit - Not applicable
Gender - Male and Female
Key inclusion criteria - A reproductive medicine specialist involved in the treatment of infertility
A reproductive medicine counselor with more than 3 years of experience in infertility nursing, or a nurse or midwife with the qualifications of a certified infertility nurse or certified reproductive nurse
A male patient who has previously undergone ART or TESE
Key exclusion criteria - Those who could not obtain written consent
Target Size - 22
Recruitment Status:
Recruitment status - Enrolling by invitation
Date of protocol fixation - 2026 Year 01 Month 11 Day
Date of IRB - 2026 Year 01 Month 23 Day
Anticipated trial start date - 2026 Year 01 Month 31 Day
Last follow-up date - 2026 Year 12 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000069771
Disclaimer: Curated by HT Syndication.
