Condition: Induction of Labor · Cervical Ripening · Cervical Ripening and Induction of Labor · Sponsor: Aalto University
The goal of this clinical study is to evaluate a new mechanical balloon catheter (INGA) used to prepare the cervix for labor induction in pregnant women at term. The study aims to assess the safety, usability, and performance of the INGA catheter when used for cervical ripening before labor. Researchers will also collect feedback from healthcare professionals and participants about the use of the device. Participants are pregnant women at term with a single baby in a head-down position who meet the study eligibility criteria. Participants will: * have the INGA balloon catheter inserted as part of labor induction, * receive standard clinical care according to hospital practice, * provide information about their experience and outcomes related to the device. The results of this study will help determine whether the INGA catheter is safe and suitable for use in cervical ripening during labor induction.
This description comes directly from the study's public registry record.
Kirsi Roivainen, Master of Health · +358 (0)50 534 7653 · kirsi.roivainen@mdsfinland.com
Heidi Kruit, MD, PhD, Assoc.prof · +358 (0)50 428 4685 · heidi.kruit@hus.fi
Always discuss trial participation with your own doctor first.
| Helsinki University Hospital | Helsinki, HUS, Finland | Recruiting |
| Hospital Nova | Jyväskylä, Finland | Recruiting |
| Tampere University Hospital | Tampere, Finland | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07414771