Correlation Between Vaginal Laxity and Delivery Mode

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorAssiut University

About this trial

Evaluation of pelvic floor using 2D and 3D Transperineal Ultrasound

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

parous women

Disqualifiers

pregnant women

previous prolapse surgery

Trial population

Parous women who have history of previous delivery either vaginal, operative vaginal or Cesarean section

Trial design

Design model

Case-crossover

Time perspective

Cross-sectional

Treatments tested in this trial

  • Transperineal Ultrasound

    Diagnostic test

    patients were asked to fill the Pelvic Floor Distress Inventory Questionnaire - Short Form 20. The imaging was performed using a GE Voluson S8 machine. A conventional linear 2D transducer (5-8 MHz) with a field of view of at least 70° was used. For tomographic or multi-slice imaging, a volumetric probe (6-8 MHz) was employed. 2D measures: Bladder neck height ( BN) , Retrovesical angle (RVA) at rest and valsalva, Bladder wall Thickness (BWT), Post micturition Residual volume. For 3D measures Measurements were analyzed offline, assessing the levator hiatal anteroposterior and transverse diameters, Levator Haital area (LHA), Pubovisceral muscle thickness at 3 and 9 o'clock, Pubovisceral muscle length, right and left levator urethral gap and urethral anal distance.

Treatment groups

150 Participants
are divided into 2 treatment groups
Group A: Group 11 intervention
Group B: Group 21 intervention

Trial outcomes

Primary outcomes

1

Levator Haital area after VD or CS

Increased area means increase vaginal laxity

Time frame
1 day

Secondary outcomes

Other outcomes

Sponsors and contacts

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