Dilapan-S/Dilasoft E-Registry in Induction of Labor

NCT02318173 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 444

Last updated 2017-05-19

No results posted yet for this study

Summary

International Observational E-Registry on the use of DILAPAN-S® osmotic dilator / DILASOFT® osmotic dilator for cervical ripening prior to labour induction.

Conditions

  • Labour Onset and Length Abnormalities
  • Labor; Forced or Induced, Affecting Fetus or Newborn

Interventions

DEVICE

Dilapan-S

Synthetic osmotic dilators Dilapan-S, Dilasoft for cervical ripening prior to induction of labor in women with unfavourable cervix

Sponsors & Collaborators

  • Medicem International CR s.r.o.

    lead INDUSTRY

Principal Investigators

  • Lars Hellmeyer, Doz, MD · Vivantes Klinikum im Friedrichshain, Berlin, Germany

  • Franz Bahlman, Doz, MD · Buerger Hospital, Frankfurt am Main, Germany

  • Janesh Gupta, MD, FRCOG · Birmingham Women´s Hospital, Birmingham, UK

  • Petr Janku, MD · Masaryk University Hospital, Brno, Czech Republic

  • Jozef Zahumensky, Doc, MD · University Hospital, Trnava, Slovakia

  • Oleg Baev, MD, PhD · Federal State Budget Institution "Research Center for Obstetrics, Gynecology and Perinatology" of the Ministry of Healthcare of Russian Federation, Moscow, RUS

  • Antonio Saad, MD, PhD · University of Texas Medical Branch Galveston, TX, US

  • Amitasrigowri Murthy, MD, PhD · Bellevue Hospital, New York City, NY, US

  • Amita Suneja, Prof, MD · Guru Teg Bahadur Hospital, New Delhi, India

  • Usha Vishwanath, MD · Sri Ramachandra Medical Center, Chennai, India

  • Anisha Gala, MD · Fernandez Hospital, Hyderabad, India

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2016-12-31
Completion
2016-12-31

Countries

  • United States
  • Czechia
  • Germany
  • India
  • Russia
  • Slovakia
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02318173 on ClinicalTrials.gov