Standard 24-hour Urine Protein vs Shorter Period for Diagnosis of Pre-eclampsia (PET and urine)

March 14, 2024 updated by: Raed Salim, HaEmek Medical Center, Israel

Comparison of the Standard 24-hour Urine Protein With Shorter Collection Periods for the Diagnosis of Preeclampsia

Background and project rationale:

Preeclampsia is a common complication of pregnancy, affecting 6-8% of all pregnancies and constitutes a leading cause of maternal morbidity and mortality. Preeclampsia is liable to endanger the lives of both the gravida and the fetus, particularly if treatment is initiated inappropriately or in an untimely fashion.

Diagnosis of preeclampsia is dependent on the finding of proteinuria, determined as being over 300mg of protein in a 24 hours urine sample. However, urine collection spanning 24 hours sometimes constitutes a "bottleneck", extending the time to diagnosis of preeclampsia. Additionally, the collection of urine for 24 hours entails a degree of discomfort, requiring that the woman be in proximity to for collection vessel, and increases the length of her hospital admission.

The use of an abbreviated test may permit diagnosis and treatment in a more timely fashion. Similarly, the ability to exclude the diagnosis more rapidly could reduce length of hospital stay and consumption of the health system's limited resources. Further, a shorter test may reduce the discomfort associated with the 24-hour test and thus increase compliance.

Previous research has suggested that briefer tests correlate with the traditional 24 hour urine collection, however these studies were based on small study populations.

Research Objective:

To validate a brief and rapid test for the diagnosis of urinary protein excretion.

To assess whether, in women with suspected preeclampsia, a difference exists between protein excretion during the daytime and at night.

Methods:

Urine collection will be performed on pregnant women admitted for investigation of suspected preeclampsia, with volumes recorded and samples taken at 6, 12 and 24 hour intervals for assessment of urinary protein content. As such, a comparison will be made between the protein excretion after 6 and 12 hours with that over a full 24 hour period; in addition, comparison will be made between daytime and nighttime urinary protein excretion. The results will allow for assessment of whether a shorter test can substitute the full 24 hour collection in the diagnosis of preeclampsia; results of women who are shown to not suffer from preeclampsia will be used to assess whether a short test can rule out the disease. Additionally a urine sample for protein/creatinine ratio will be examined and correlated with results of the different collection periods.

Study Overview

Status

Completed

Conditions

Detailed Description

Literature review and project rationale:

Preeclampsia is a common complication of pregnancy, affecting 6-8% of all pregnancies and constitutes a leading cause of maternal morbidity and mortality. Preeclampsia is liable to endanger the lives of both the gravida and the fetus, particularly if treatment is initiated inappropriately or in an untimely fashion.

The diagnosis of preeclampsia is based on findings of raised blood pressure (over 140/90mmHg) and the presence of proteinuria. The accepted means of measuring proteinuria is by 24-hour urine collection, with a pathological value defined as 300mg or greater in the 24 hour period. When the proteinuria is greater than 5000mg in 24 hours, the pr-eclampsia is classified as severe and is further endangers the lives of the expectant mother and fetus and often results in early delivery.

Diagnosis and assessment of severity of preeclampsia require a timely situation assessment. Urine collection spanning 24 hours sometimes constitutes a "bottleneck", extending the time to diagnosis of preeclampsia. Additionally, the collection of urine for 24 hours entails a degree of discomfort, requiring that the woman be in proximity to for collection vessel, and increases the length of her hospital admission.

The use of an abbreviated test may permit diagnosis and treatment in a more timely fashion. Similarly, the ability to exclude the diagnosis more rapidly could reduce length of hospital stay and consumption of the health system's limited resources. Further, a shorter test may reduce the discomfort associated with the 24-hour test and thus increase compliance.

Previous research has shown that 8-hour urine collection does indeed produce results paralleling the 24-hour collection, and recent research also demonstrates concordance between 12-hour and 24-hour urine collections. That said, both these studies were based on small sample populations, fewer than 100 women. Another study of women with preeclampsia showed good correlation between the results of urinary protein in samples collected over 12 hours at night and those collected over 12 hours during daytime.

Research Assumptions:

  1. urine collection for a period of time less than 24 hours will reflect the degree of urinary protein excretion.
  2. urine collection for a period of time less than 24 hours will constitute an alternative test for 24-hour urine collection, the accepted diagnostic test today.

Research Objective:

To validate a brief and rapid test for the diagnosis of urinary protein excretion.

To assess whether, in women with suspected preeclampsia, a difference exists between protein excretion during the daytime and at night.

Methods:

Urine collection is to be performed on every pregnant admitted for investigation of suspected preeclampsia. After 6, 12 and 24 hours samples of the collected urine will be taken for protein concentration assessment. Quantitative urinary protein will be established according to urinary protein concentration and collected urine volume. Results of the tests after 6 and 12 hours will be compared to the final results after 24 hours, that being the test of choice for diagnosis of proteinuria in preeclampsia and thus the test that will determine management (according to department protocol).

Women for whom preeclampsia has been ruled out (viz, those who underwent investigation following raised BP but without a finding of proteinuria) will serve to assess the ability of a short urine collection to rule out proteinuria and, as such, preeclampsia.

So as to assess whether there is a difference between results of daytime urinary protein excretion and those at night, the urine collection will be performed in two vessels as follows:

  1. 8:00am - beginning of urine collection
  2. 2:00pm, vessel 1 - recording of collected urine volume, removal of a 10mL sample of urine for protein concentration testing.
  3. 8:00pm, vessel 1 - recording of total collected urine volume, removal of a 10mL sample of urine for protein concentration testing.

    at this point urine collection will be continued in the second vessel

  4. 8:00am the following morning, vessel 2 - recording of collected urine volume as of 8:00pm (the previous 12 hours), removal of a 10mL sample of urine for protein concentration testing.
  5. contents of the two vessels are mixed, 24 hour urine volume recorded and a 10mL sample taken, this being the sample that will establish the result of the 24 hour urine collection.

Additionally a urine sample for protein/creatinine ratio will be examined and correlated with results of the different collection periods.

Study Type

Observational

Enrollment (Actual)

307

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Afula, Israel
        • HaEmek Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 55 years (Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

pregnant women admitted for assessment of suspected preeclampsia

Description

Inclusion Criteria:

  • pregnant women
  • age 18-55 years
  • blood pressure >140mmHg systolic or >90mmHg diastolic

Exclusion Criteria:

  • known renal disease
  • urinary tract infection
  • spontaneous labor or need to induce labor within the first 24 hours of admission

Study Plan

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

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
to validate a shorter urine collection time for assessment of proteinuria
Time Frame: one year
urine collection over 6 and 12 hours to compare with results of the official 24 hours urine collection for proteinuria in the investigation of suspected preeclampsia
one year
To examine if a shorter urine collection time for assessment of proteinuria is comparable to the standard 24 hours
Time Frame: one year
one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Raed Salim, M.D., HaEmek Medical Center

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2013

Primary Completion (Actual)

July 1, 2023

Study Completion (Actual)

August 1, 2023

Study Registration Dates

First Submitted

June 11, 2013

First Submitted That Met QC Criteria

June 17, 2013

First Posted (Estimated)

June 19, 2013

Study Record Updates

Last Update Posted (Actual)

March 15, 2024

Last Update Submitted That Met QC Criteria

March 14, 2024

Last Verified

August 1, 2022

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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