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Evaluation of Levator Injuries Using Transvaginal Endosonography (ELITE)

C

Croydon University Hospital

Status

Completed

Conditions

Childbirth Related Levator Injuries

Study type

Observational

Funder types

Other

Identifiers

NCT01310660
10/H0806/87

Details and patient eligibility

About

Prospective studies to date have identified that the levator ani muscle injuries occur in 14-19% of women after vaginal delivery.

In none of studies a vaginal examination was performed at the time of delivery. It has previously been shown that sonographic injuries of the anal sphincter that were believed to be occult were in fact clinically apparent but not recognised at the time of delivery. It is therefore important to correlate clinical findings to ultrasound images.

3D endovaginal endosonography has not previously been used to identify levator injuries. This should potentially provide a better view of the pelvic floor muscles.

The relationship between levator injury and symptoms of pelvic floor dysfunction has not been previously established using validated questionnaires. In this study, we include validated questionnaires to evaluate urinary incontinence, faecal incontinence and vaginal symptoms. As symptoms may become apparent only in the long term it is prudent that the women are followed up in the long term.

The principle objective is to establish the incidence of levator muscle defects during pregnancy and after childbirth. The levator muscle forms a major part of the pelvic floor and damage to this muscle can potentially cause urinary, bowel and sexual problems and pelvic organ prolapse.

Enrollment

269 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Pregnant women who have not delivered previously
  2. Singleton pregnancy
  3. Maternal age > 18 years and
  4. No previous pregnancies >20 weeks of gestation
  5. Ability to read and understand English.

Exclusion criteria

  1. Pregnant women who have delivered previously
  2. Multiple pregnancies

Trial design

269 participants in 1 patient group

Nulliparous

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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