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Clinical Trials/NL-OMON43713
NL-OMON43713
Completed
Not Applicable

Maternal and offspring outcomes after treatment of hyperemesis by refeeding - MOTHER Trial

Academisch Medisch Centrum0 sites120 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
hyperemesis gravidarum (HG)
Sponsor
Academisch Medisch Centrum
Enrollment
120
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Gestational age between 5\+0 and 19\+6 weeks
  • Informed consent
  • Women with singleton or multiple pregnancy
  • Hospital admission because of hyperemesis gravidarum (the diagnosis of HG is made if excessive nausea or vomiting necessitates admission)
  • First admission or readmission for hyperemesis gravidarum

Exclusion Criteria

  • Maternal age \< 18 years
  • Mola hydatidosa
  • Non\-vital pregnancy
  • acute infection causing vomiting (acute appendicitis, pyelonephritis)
  • Contra indication for enteral tube feeding (including esophageal varices, allergies to compounds in enteral mix)
  • HIV infection

Outcomes

Primary Outcomes

Not specified

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