Completed

Water Immersion and Changes in the Fetoplacental Circulation. A Case-Control Study With the Case as it's Own Control.

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What is being tested

Immersion into water

Other
Who is being recruted

Over 18 Years
+14 Eligibility Criteria
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How is the trial designed

Treatment Study

Interventional
Study Start: February 2011
See protocol details

Summary

Principal SponsorHvidovre University Hospital
Last updated: February 26, 2013
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 2011

Actual date on which the first participant was enrolled.

Intrauterine growth retardation and preeclampsia are major causes of neonatal mortality, morbidity and later neurological sequelae. The conditions are associated with an increased resistance to blood flow in the placenta, that can be detected by an increase in pulsatility index (PI) in the umbilical artery (1). When Doppler flow is assessed in the uterine arteries, increased resistance in the uteroplacental circuit is indicated both by an increase in PI and by a change in the flow velocity waveform, which can be seen as a "notch" in early diastole. In the 2nd trimester, the invasion of trophoblasts and the remodeling of the uterine spiral arteries are complete. Persistence of a bilateral notch beyond the 24th week of gestation is associated with an increased risk of intrauterine growth retardation and preeclampsia. Even though the risk persists, the notch usually disappears later in pregnancy (2). When the non-pregnant body is immersed in water, extracellular fluid is redistributed back into the circulation. Central blood volume, cardiac output, renal perfusion and urine output increase and the blood pressure falls (3-7). The same changes occur in the pregnant women. However the increased diuresis is strongly correlated with the degree of the pregnancy edema, which decreases substantially (8), and the amount of amniotic fluid increases (9). The changes all occur within minutes (8), but are transient and return to conditions before immersion within 1-2 hours after the pregnant woman has come out of the water. The changes in the above parameters are significant but less pronounced in pregnant women with preeclampsia than in pregnant women without the condition (11). None of the experiments showed changes in the fetal heart rate. Because of the physiological changes that take place when pregnant women are immersed in water, several authors have speculated whether immersion has a positive effect on the uteroplacental circuit (8,10,12). There are no published data on Doppler flow measurements in the umbilical artery and the uterine arteries during water immersion. The aim of the present study is to evaluate the effect of immersion on the fetoplacental and uteroplacental circuits in healthy pregnant women, using Doppler flow measurements in the umbilical artery and uterine arteries. Materials From the Department of Obstetrics and Gynecology, Hvidovre University Hospital, Denmark, we recruit 25 healthy women with an uncomplicated singleton pregnancy. Gestational age was between 26 and 38 weeks. All participants will have a normal first trimester combined screening and a normal second trimester ultrasound scan for fetal abnormalities. Within the last 2 weeks prior to participation, fetal weight will be estimated, and only woman with fetuses of normal weight (within the 95 percentile) will be included. Methods The study is performed at the labor ward at Hvidovre Hospital, Denmark. If fetal weight has not been estimated by an ultrasound examination within the last 2 weeks, fetal weight will be estimated on the day of the study. In order to exclude an on-going infection, the temperature is measured and the urine examined in all participants on the day of the study. The same experienced sonographer performs all examinations, and the same Bruel & Kjaer ultrasound scanner, suitable for scanning under water, is used in all participants. Each participant has five recordings of blood pressure, pulse, saturation, deepest vertical pocket (DVP) of amniotic fluid and Doppler flow in the umbilical artery and uterine arteries. All recordings are obtained during the same study session. Doppler ultrasound measurements of umbilical and uterine arteries are obtained by pulsed wave ultrasound using an insonating angle as close to 0 degrees as possible. The Doppler measurements on the uterine arteries are obtained approximately one centimeter from the crossing of the iliac arteries. The pulsatility index (PI) is calculated automatically by the machine using the formula (systolic velocity-diastolic velocity)/mean velocity. PI of the uterine artery is calculated as the mean PI of the left and the right uterine artery. For immersion, a regular bathtub is used. The tub is filled with thermo-neutral tap water (35.0 °C +/- 0.5 °C). The temperature of the water is measured every 10 minutes, and kept thermo-neutral during the period of immersion. The participants are placed in a supine position outside the bathtub and the first recordings are obtained (T0). Afterwards the participants are immersed in water, placed in a supine position, and measurements are repeated after 5 min (T5) and 25 min (T25) in water. All measurements are repeated with the participant in a supine position outside the bathtub 15 min (T40) and 30 min (T55) after immersion. All recordings of Doppler flow curves and measurements of amniotic fluid (DVP) are saved on an USB stick. An experienced specialist in fetal medicine, who is not present at the investigation, validates each recording blindly. Any recording not eligible for approval is redefined as a missing value. Statistical analysis Because the measurements taken before, during and after immersion, are made in the same patient during the same study session, and with the same ultrasound apparatus, each participant act as their own control. Data are expressed as means +/- standard error of the mean (SEM). The first recording, T0, was defined as baseline. Comparisons between the respective recordings, T0-T55, are done using a two-tailed paired t-test on raw data. P-values < 0.05 are considered significant. For calculation, STATA 12.1 (13) is used.

NCT01799343
Principal SponsorHvidovre University Hospital
Last updated: February 26, 2013
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

25 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Female

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

4 inclusion criteria required to participate
Normal first trimester combined screening

Normal second trimester ultrasound scan for fetal abnormalities

Normal weight fetuses

Singleton pregnant women

10 exclusion criteria prevent from participating
Abuse of medication, alcohol- or drugs

Body mass index above 35

Cardiovascular disease

Cerclage

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Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Normal healthy singleton pregnant women. The case serves as its own control. Measurements of mean arterial pressure, deepest vertical pocket of amnion fluid and Doppler flow in the umbilical and uterine arteries will be assessed before immersion (Baseline), during immersion (Immersion) and after immersion (Post-immersion).

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Dep. Gynaecology and Obstetrics, Hvidovre University Hospital

Hvidovre, DenmarkOpen Dep. Gynaecology and Obstetrics, Hvidovre University Hospital in Google Maps
CompletedOne Study Center