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PregnancyDEUNCT02283567

The Difference Between Elasticity of the Uterine Cervix in Singleton and Twin Pregnancies

An observational study of Pregnancy, run by Meir Medical Center.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The investigators aim to compare elasticity of the uterine cervix in singleton and twin pregnancies of similar gestational age. Read more about this study

Who is it for?
Ages 20 to 44 years, women onlyHealthy volunteers can take part
Conditions the study is for
Pregnancy
How many people
40 participants
Where
No sites listed yet
Study dates
Nov 2015to Nov 2016
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 44 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Study population: 20-44 years old pregnant patients

Who may be able to join

  • Low risk singleton and twin pregnancies

Who cannot join

  • Patients with pregnancy complications

Trial locations and contacts

No sites are listed yet.

About this study

The investigators aim to compare elasticity of the uterine cervix in singleton and twin pregnancies of similar gestational age.

Read the detailed description

Softening of the uterine cervix occurs during pregnancy.There is a possibility that this process occurs earlier in twin versus singleton pregnancies.The softening of the cervix is reflected by the level of its elasticity which can be measured sonoelastographically. A two dimension image of the cervix is obtained in the midsagittal section and the length is noted. A 2nd sonoelastography image is obtained before pressure is applied with the transducer in the area of the internal os and a third sonoelastography image is obtained until no more shortening of the anterior-posterior diameter is observed.Elastography measurements of the internal os are performed using a color map: red (soft), yellow (medium soft), blue (medium hard) and purple (hard) before and after the application of strain.The change between the color maps before and after strain application in singleton pregnancies will be compared to the change in twin pregnancies of similar gestational age.

Conditions
Pregnancy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Comparison of elasticity levels in singleton and twin pregnancies (Elastographic measurements of the internal os)

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Nov 2014 (estimated)
  2. Study startNov 2015
  3. Primary completionNov 2016 (estimated)
  4. Study completionNov 2016 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02283567
Sponsor's protocol ID
0152-14-MMC
Acronym
DEU
Status last verified
Sep 2015
First submitted
27 Oct 2014
Last updated
23 Sep 2015
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Pregnancy, run by Meir Medical Center.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 23 Sep 2015. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Rami Aviram, MD (972544944862, rami.aviram@clalit.org.il), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Comparison of elasticity levels in singleton and twin pregnancies (Elastographic measurements of the internal os) (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Sep 2015.

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