Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:01 PM
Ignite Modification Date:
2025-12-24 @ 1:01 PM
NCT ID:
NCT00795561
Eligibility Criteria:
Inclusion Criteria:
Women (no age limits) will be admitted to the study if they have two or more of the following criteria
* Ongoing viable intrauterine pregnancy/ pregnancies \< 22 weeks gestation
* Persistent vomiting (\>x3 episodes/ 24 hours) not attributable to other causes
* Severe nausea not attributable to other causes.
* Dehydration diagnosed by the presence of ketonuria.
* Electrolyte imbalance not attributable to other causes.
Exclusion Criteria:
Women will not be admitted to the study if any of the following criteria are present.
* Women with a confirmed urinary tract infection (mid stream urine isolation of a single strain of uropathogen \>105 bacteria/ml)
* Women with molar pregnancies
* Women with non viable pregnancies.
* Women who have already received treatment for NVP outside of this trial.
* Pregnant women who present who will not be booking at CUMH for their pregnancy or are not resident in the South West of Ireland i.e. day care treatment is not an option.
* Women who do not have a good understanding of English.
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT00795561
Study Brief:
Protocol Section:
NCT00795561