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NCT02983240

Electrical Inhibition of Human Preterm Contractions

Suspended NA Last updated 4 December 2024
What this trial tests

NA trial testing Electrical Uterine Pacemaker in Preterm Labor in 110 participants. Suspended.

Timeline
1 March 2017
Primary endpoint
21 January 2026
21 January 2026

Quick facts

Lead sponsore-Bio Corp
PhaseNA
StatusSuspended
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment110
Start date1 March 2017
Primary completion21 January 2026
Estimated completion21 January 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

e-Bio Corp

Who can join

Adults 18 to 50, female only, with Preterm Labor or PreTerm Birth. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to explore a new method to stop preterm uterine contractions using an electrical device. The device, an "electrical pacemaker for the uterus," has been approved by the Food and Drug Administration (FDA) for clinical research in pregnant women. The purpose of this study is to evaluate the feasibility and safety of the device. The investigators hypothesize that human preterm uterine contractions can be safely and objectively inhibited with a weak electrical current provided by an electrical inhibition (EI)/uterine pacemaker device, and that this effect relates to the timing and length of EI exposure.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Preterm Labor

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02983240.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing