Chewing Gum Containing Vitamin-c to Treat Emesis Gravidarum

The following 3 groups of patients should be compared: (1) patients with emesis gravidarum who take a chewing gum with vitamin C (verum) "ad libitum" several times daily for 2 weeks; (2.) patients with emesis gravidarum who take chewing gum without vitamin C (placebo) "ad libitum" several times daily for 2 weeks; (3.) patients with emesis gravidarum who do not use chewing gum during the study phase. The enrollment will take place at the Department of Obstetrics and Gynecology, Division of Obstetrics and Feto-Maternal Medicine, at the Medical University of Vienna. All pregnant women in the first trimester, who present for triage and birth registration between 6 to 9 gestational weeks, complaining of nausea and meeting the inclusion criteria, will be offered to participate in the study. If they agree to participate, patients will be randomized to one of the 3 study groups. In case of enrollment, patients are not allowed to take any other nausea therapy during the study period, otherwise the results could be distorted. Both the vitamin C-containing chewing gums (verum) and the non-vitamin C-containing chewing gums (placebo) are manufactured by the company Frey AG (Migros-Genossenschafts-Bund, 8031 Zurich, CH). Both chewing gums are not distinguishable from each other in taste. The only difference between verum and placebo is the proportion of 150mg vitamin C per chewing gum (for verum) or no vitamin C (for placebo). The other ingredients are as follows: sweeteners isomalt, sorbitol, maltisirup, sucralose, acesulfame K, chewing gum (with antioxidant E306), sodium L-ascorbate, flavorings, acidifier (apple and citric acid), thickener gum arabic, dye E171, humectant E422 and E1518, coating agents E903 and E553b. The randomization takes place by means of the GCP-compliant web-based randomizer of the Institute of Medical Informatics, Statistics and Documentation (IMI) of the Medical University of Graz (license Meduni Vienna). The ratio of the allocation to the 3 groups is 1:1:1. Furthermore, as co-variable nicotine abuse is included in the randomization, since smoking with a lower risk correlates with suffering from hyperemesis gravidarum. Study patients are asked to complete a validated questionnaire (modified PUQE-Score) on their condition. In addition, there is a blood sample for the determination of diamine oxidase (DAO) and the histamine concentration in the blood of the patient. Patients are subsequently evaluated at two further follow-up appointments, one in the course of routine retesting for cervical crease measurement (between 11-14 weeks of gestation) and 2nd time during routine organ screening (between 20-24 weeks of gestation). At these appointments, a blood sample for the determination of DAO and the evaluation of well-being using the Modified PUQE questionnaire are carried out again. With the second control appointment the supervision ends within the study. The study phase is thus completed at the latest at the time of the organ screening at the Department of Obstetrics and Gynecology, at the latest until the 24th week of pregnancy. For the determination of DAO and histamine, the following tubes (a total of 16mL blood) are necessary: 1 serum tube of 8mL with separating gel (DAO) + 1 EDTA tube of 8mL (histamine). In addition, it is planned to store the material that has not been used for the determination of DAO and histamine in order to answer future questions in the field of biomedical research in the MedUni Vienna Biobank. The legal basis for this can be found in the Research Organization Act 2018 §2d. For each additional project that uses samples and / or data from this study, a separate report will be sent to the Ethics Committee of the Medical University of Vienna. The analysis of the DAO levels takes place in the Allergy Center Floridsdorf, which has many years of experience in the measurement of DAO and is considered a reliable partner. The samples are pseudonymized and stored at -80°C. The measurement of histamine concentration is carried out by the Clinical Institute for Laboratory Medicine at the Medical University of Vienna. The samples are taken directly after acceptance by means of a cooled transport container on site for analysis (coordinated preanalytics). The design of the planned study is prospective, randomized, double-blind, placebo-controlled. Blinding is provided between verum and placebo chewing gum (groups 1-2). The taste of verum and placebo chewing gum is identical. The non-inferiority of chewing gum cooking against doing nothing should also be proved. In addition to the course of objective parameters such as DAO and histamine, the personal condition of the affected patient should be assessed on the basis of the modified PUQE score. The number of ingested chewing gum is determined by means of the number of used packs on the 1st inspection date. In addition, maternal characteristics are collected, which should be descriptive and should be included in the multivariate model: age, pregnancy, parity, gestational age at diagnosis, comorbidities, long-term medication, complications in this or previous pregnancies, previous hyperemesis gravidarum, nicotine abuse, educational level. In addition, the pregnancy outcome is retrospectively assessed in order to evaluate any influence of the chewing gum containing vitamin C on the pregnancy outcome. The primary endpoint is the modified PUQE score for the 1st control appointment. Secondary endpoints are the PUQE score at the 2nd control appointment, as well as DAO and histamine concentrations for the 1st and 2nd control appointment. About the statistical methods: Based on the work of Birkeland E et al., a standard deviation of 3 points or less can be assumed for each Modified PUQE score group. With a caseload of 45 patients per group, the ANCOVA has a power of> 80% to find a difference between the three groups if two groups differ by at least 2 points. For the pairwise comparisons, the same difference results in a power of 88%. With a correction for a drop-out rate of 10%, this results in a case number of 50 patients per group. Descriptive statistics (number, mean, standard deviation, median, minimum and maximum) should be given separately for the 3 target variables Modified PUQE score, DAO and histamine values for the 3 measurement times. The data is also displayed graphically using box plots and trajectories. Further metric variables are also described by mean, standard deviation, median, minimum and maximum, categorical variables are described by absolute and relative frequencies. As a primary analysis, a mean value comparison of the Modified PUQE scores is performed between the 3 groups for the measurements at the 2nd control date. For this, an ANCOVA model is calculated, to which the respective initial values at birth registration and the week in which the second measurement takes place are considered as covariates. From the ANCOVA model, the null hypothesis that there are no group differences on average is tested with an F-test at the 5% significance level. If this global null hypothesis is discarded, all pairwise group comparisons are performed by T tests for the corresponding model coefficients of the ANCOVA model at the 5% significance level. This test procedure does not require any further correction for multiple testing when comparing 3 groups. In another exploratory model, the maternal characteristics listed in the preceding section are additionally included as covariates to investigate the potential influence of these variables on the Modified PUQE score and to calculate adjusted group differences. The secondary endpoints are compared to the primary endpoint using ANCOVA models between the three groups. As a further secondary analysis, the Spearman correlations between the Modified PUQE scores, DAO and histamine levels at the three different time points will be determined.