%0 Generic %A Samenjo, Karlheinz %A Ramanathan, Aparna %A Gwer, Stephen %A Bailey, Robert %A Imbamba, Javan %A Odenyo, Stella %A Koksal, Erin %A Omoto, Jackton %A Mak'Otieno, Fredrick %A Diehl, Jan Carel %D 2024 %T Data  underlying the publication: Validation of a novel medical device (Chloe SED®) for the administration of analgesia during manual vacuum aspiration: a randomized controlled non-inferiority pilot study %U %R 10.4121/7e08e77b-f4a9-4054-81a5-e83b7946cb21.v1 %K Clinical trial %K medical device design %K paracervical block %K manual vacuum aspiration %K abortion care %X

This dataset assesses the efficacy of Chloe SED®, a novel device for administering analgesia during manual vacuum aspiration (MVA), through a multisite, randomized controlled non-inferiority trial aimed at comparing its effectiveness to the standard spinal needle in providing humane care for abortion or miscarriage procedures in low-resource Kenyan healthcare settings. Data captures patient pain tolerance and experiences with Chloe SED® versus the spinal needle, gestational age, prior MVA experiences, reasons for MVA, as well as healthcare providers’ perceptions of pain control and their experience with MVA procedures. The dataset enables a comprehensive comparison of pain control outcomes between Chloe SED® and the standard method, providing insight into the device's potential for improving care quality.

%I 4TU.ResearchData