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Hyperemesis Gravidarum clinical trials

View clinical trials related to Hyperemesis Gravidarum.

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NCT ID: NCT02163434 Completed - Clinical trials for Hyperemesis Gravidarum

Comparison of Gabapentin and Metoclopramide for Treating Hyperemesis Gravidarum

Start date: June 2014
Phase: Phase 2
Study type: Interventional

The investigators will compare the effectiveness of gabapentin to metoclopramide for 1 week among 60 women with hyperemesis gravidarum (HG) in this randomized, double-blinded trial. After completion of the 1-week double-blind phase, subjects will be offered open-label gabapentin with rescue metoclopramide until their symptoms no longer require treatment. Enrollment will occur at the University's at Buffalo, of Rochester and of Wisconsin.

NCT ID: NCT01836835 Completed - Clinical trials for Hyperemesis Gravidarum

Pregnancy Specific Nausea Questionnaire (PUQE) Translated and Tested in Norwegian

PUQE-N
Start date: May 2013
Phase: N/A
Study type: Observational [Patient Registry]

Nausea in early pregnancy (emesis gravidarum) is very common but most often self-limiting. Hyperemesis gravidarum; where nausea and vomiting is severe and protracted is potentially dangerous for the woman and her foetus and necessitates hospital treatment. An English questionnaire (PUQE; Pregnancy Unique Questionnaire of Emesis) exists that can differentiate between uncomplicated emesis and the severe hyperemesis condition. This questionnaire has been translated to Norwegian. The investigators want to test the ability of this questionnaire to differentiate the grade of nausea/vomiting between a group of presumed normal pregnant woman and patients treated for hyperemesis gravidarum in a Norwegian population. The investigators also want to relate the PUQE questionnaire scoring to the women/patients' self-reported nutritional intake during 24 hours.

NCT ID: NCT01559012 Completed - Clinical trials for Hyperemesis Gravidarum

Transdermal Clonidine in the Treatment of Severe Hyperemesis Gravidarum

CLONEMESI
Start date: February 2012
Phase: Phase 3
Study type: Interventional

CLONEMESI is an academic, independent, randomized placebo-controlled trial to assess the effect of transdermal (TD) clonidine in improving the symptoms of severe Hyperemesis Gravidarum(HG) affecting women in their 6th-12th week of pregnancy. The study has a crossover design.

NCT ID: NCT00861523 Terminated - Clinical trials for Hyperemesis Gravidarum

Does Thiamine Help Vomiting and Nausea in Pregnancy?

Start date: February 2009
Phase: Phase 3
Study type: Interventional

There are different treatments for nausea and vomiting in pregnancy. According to the ACOG recommendations, promethazine is the first line of parenteral treatment after oral treatment had failed. Thiamine is given to prevent wernicke encephalopathy. This research try to find out whether thiamine helps the vomiting and nausea as well, by comparing the response to thiamine and promethazine in women who suffer from nausea and vomiting in pregnancy.

NCT ID: NCT00795561 Completed - Pregnancy Clinical Trials

Management of Nausea and Vomiting of Pregnancy

DIM
Start date: April 2009
Phase: N/A
Study type: Interventional

Upto 80% of all pregnant women experience some form of nausea and vomiting (NVP) during their pregnancy. Hyperemesis gravidarum, a more severe form of NVP affects approximately 0.3- 2.0% of pregnancies and is the commonest indication for admission to hospital in the first half of pregnancy and second only to preterm labor as a cause of hospitalization overall. According to the Hyperemesis Education and Research Foundation, conservative estimates indicate that HG can cost a minimum of $200 million annually in house hospitalizations in the United States of America. The investigators aim to conduct a randomized controlled trial to test the hypothesis that the availability of day care services for the initial treatment of NVP reduces the mean duration of stay in hospital by 1 day and results in significantly greater patient satisfaction compared with standard inpatient management.

NCT ID: NCT00293644 Completed - Pregnancy Clinical Trials

Pre-emptive Treatment of Severe Nausea and Vomiting of Pregnancy

Start date: February 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether pre-emptive use of a delayed release combination of pyridoxine hydrochloride and doxylamine succinate (Diclectin®), before eruption of symptoms of Nausea and vomiting of pregnancy and hyperemesis gravidarum, will reduce the incidence of severe forms of this syndrome/HG.