Tokyo, July 23 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058504) titled 'Prospective Comparison Study of a Noninvasive Finger-Cuff Device for the Prevention of Hypotension During Cesarean Delivery Under Spinal Anesthesia' on July 22.
Study Type:
Interventional
Study Design:
Basic Design - Parallel
Randomization - Randomized
Blinding - Open -no one is blinded
Control - No treatment
Primary Sponsor:
Institute - Kindai University
Condition:
Condition - Pregnancy
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To Evaluation of the Utility of Noninvasive Finger-Cuff Monitoring for the Prevention of Hypotension During Cesarean Delivery Under Spinal Anesthesia
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - Evolution of blood pressure with a non-invasive finger cuff in operation room
Interventions/Control_2 - none
Eligibility:
Age-lower limit - 18
years-old
<=
Age-upper limit - Not applicable
Gender - Female
Key inclusion criteria - Pregnancy female over 35 weeks gestation
Key exclusion criteria - No agreement
Target Size - 110
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2025 Year 07 Month 07 Day
Anticipated trial start date - 2025 Year 08 Month 01 Day
Last follow-up date - 2026 Year 12 Month 01 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066888
Disclaimer: Curated by HT Syndication.
