Electrical Inhibition (EI): A Preliminary Study To Inhibit Preterm Labor And Preterm Birth
Public ClinicalTrials.gov record NCT02569216. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Electrical Inhibition (EI): A Preliminary Study To Prevent The Uterine Contractions Of Human Preterm Labor And Preterm Birth
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
An electrical-inhibition (EI) uterine pacemaker device similar to an electrical heart pacemaker delivers a weak electrical current to the human uterus during active preterm labor to rapidly and safely inhibit the unwanted premature uterine contractions and possibly a preterm birth.
Study identification
- NCT ID
- NCT02569216
- Recruitment status
- Withdrawn
- Study type
- Interventional
- Phase
- Phase 1
- Enrollment
- Not listed
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 18 Years to 55 Years
- Sex
- Female
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Feb 8, 2016
- Primary completion
- Aug 14, 2016
- Completion
- Aug 14, 2016
- Last update posted
- Nov 8, 2017
2016
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| New York University Hospital | Manhattan | New York | 10016 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Recently updated Premature Birth trials
Other public records listing Premature Birth. Sorted by last update posted; newest first. Not a recommendation.
- NCT07570121: Pharmacokinetics and Placental Transfer of Caffeine Recruiting
- NCT06036446: LATe Cerclage in High-risk Pregnancies (LATCH) Recruiting
- NCT05264779: The Periviable GOALS Decision Support Tool Recruiting
- NCT05685745: Multisite Inventory of Neonatal-Perinatal Interventions (MINI) Minimum Dataset Recruiting
- NCT05341960: Nourishing Beginnings: Addressing Food Insecurity During Pregnancy Active, not recruiting
- NCT05204719: Prophylactic DR-CPAP on Late Preterm Infants Born by C-section: an RCT Active, not recruiting
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT02569216, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Nov 8, 2017 · Synced Sep 9, 2026
Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.
Open the official record
The complete protocol, eligibility criteria, and contact information for NCT02569216 live on ClinicalTrials.gov.