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NCT04451109Active, not recruiting

Dilapan-S®: A Multicenter US E-registry

Source: ClinicalTrials.gov · Last updated 22 Nov 2024

Brief summary (registry, in English)

Objective of this registry is to collect a representative set of real world data on the use of Dilapan-S® for pre-induction cervical ripening in daily clinical practice. Upon completion of the registry, relevant collected data will be analyzed and published.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
1200 (estimated)
First submitted
17 Jun 2020
Start date
1 Dec 2020
Primary completion date
31 Dec 2024
Lead sponsor
Medicem Technology s.r.o.
NCT number
NCT04451109

What you commit to

  • Study type: Observational
  • Planned participants: 1200
  • From 1 Dec 2020 to the primary completion date, 31 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Data not available for extraction

Who the study is looking for

  • Pregnant woman whose plan of care is induction of labor
  • Maternal age ≥ 18 years
  • Gestational age ≥ 37 +0/7 weeks
  • Dilapan-S® used for cervical ripening

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The University of Texas Medical Branch
Coordinator of this site? Confirm its status
GalvestonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.