Open, Randomized Feasibility Trial on the Safety and Performance of the INGA Catheter for Labor I… (NCT07214948) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Open, Randomized Feasibility Trial on the Safety and Performance of the INGA Catheter for Labor Induction
40 participantsStarted 2026-05
Plain-language summary
This study investigates the safety and usability of the new INGA catheter for labor induction.
Labor induction is common, with about one in three births being induced. In this study, the INGA catheter will be compared to a currently used method. The INGA catheter is a single-balloon device that works similarly to a Foley catheter but is made from different materials. Feedback will be collected from both healthcare professionals and participating women.
Who can participate
Age range
18 Years – 56 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Pregnant women aged ≥18 and ≤56 years
* An unripe cervix, ≤6 points according to the Bishop score assessment (0-10-point scale)
* Planned induction of labor by balloon catheter method
* Gestational age at the time of the study ≥ 37 weeks (gestational age confirmed by ultrasound before the 21st week of pregnancy)
* Singleton pregnancy
* Cephalic presentation
* The subject understands the study information and signs the informed consent
Exclusion Criteria:
* Preterm induction of labor (\<37 weeks of gestation)
* Abnormal Cardiotocography (CTG) at inclusion
* Spontaneous rupture of membranes at inclusion
* Clinically significant vaginal bleeding with a need of hospitalization in the third trimester
* Clinical active vaginal or uterine infection
* Maternal Human Immunodeficiency Virus (HIV), hepatitis C, or hepatitis B
* Uterine scar (including previous cesarean section)
* Condition requiring immediate delivery of the fetus or mother
* Presence of eclampsia
* Severe Preeclampsia \[Blood pressure (BP)≥ 160/110 and any of the following: thrombocytopenia with platelet count \<100 × 10e9/L, HELLP- syndrome ( Hemolysis, Elevated Liver enzymes and Low Platelets), progressive renal insufficiency, pulmonary edema \]
* Severe fetal growth restriction (Fetal Growth Restriction (FGR) fetal growth \<-2 SD/\<10th percentile)
* Estimated fetal weight ≥ 2 Standard Deviation /≥ 95th percentile
* Reduced amniotic fluid volume (deepest vertical pocket \<30 mill meter)
* Br…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.