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Dilapan-S / Dilasoft E-Registry in Induced Abortion — DSREGISTRYIA  

Abortion, Induced Clinical Trial

Official title:
International Observational E-Registry on the Use of Dilapan-S/Dilasoft Osmotic Dilators for Cervical Priming Prior to Induced Abortion

Clinical Trial Summary

International Observational E-Registry on the use of osmotic dilators DILAPAN-S® / DILASOFT® for cervical priming prior to induced abortion.

Clinical Trial Description

International, multicentre, non-interventional, observational e-registry, post market clinical follow up study to document current clinical use of Dilapan-S or Dilasoft for cervical priming before induced abortion with regard to the number of dilators used, duration of insertion of dilators in situ and unusual complications consequent of their use. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02318212
Study type Observational
Source Medicem International CR s.r.o.
Contact
Status Completed
Phase N/A
Start date March 2015
Completion date December 2016
View Details
See also
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