Repair by Rehabilitation of Pelvic Floor Lesions After Vaginal Delivery Identified by Transperineal Ultrasound 3/4 D

Physical Activity Clinical Trial

Official title:

Repair by Rehabilitation of Pelvic Floor Lesions After Vaginal Delivery Identified by Transperineal Ultrasound 3/4 D

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03686956
• Other study ID #: Rehabilitation of the avulsion
• Status: Completed
• Phase: N/A
• Start date: August 1, 2018
• Est. completion date: June 1, 2019

Study information

• Verified date: August 2020
• Source: Hospital Universitario de Valme
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

SUMMARY: (Objective, design, scope of the study, subjects of study, instrumentation, results, conclusions)

Objectives: To evaluate if the physiotherapy treatment in pelvic floor dysfunctions, identified by transperineal ultrasound 3 / 4D, in postpartum improve the tone and functionality of pelvic floor.

Design: Post-authorization, prospective, longitudinal randomized intervention study

Scope: Full-term deliveries at the University Hospital. Subjects of study: Full-term primiparous and full-term pregnancies with pelvic floor lesion, identified by transperineal ultrasound 3 / 4D, which are randomized between the physiotherapy treatment of pelvic floor and the non-work.

Variables: Primary variable: Assess the improvement in contractility / tone, evaluation by manometry and assess the anatomical improvement of the area of ?? the genital hiatus, stay by transperineal ultrasound 3 / 4D. Secondary variables: Identify the levator ani muscle injury rate, estimate the sonographic changes in the levator ani muscle through rehabilitation. Analyze the improvement of the symptoms associated with the public organic prolapse and evaluate the improvement of the quality of life.

Data analysis: To detect a difference of 10% in the reduction of the size of the index between the study groups (not intervened / intervened) after 6 months of intervention, standard deviation 10%, Error-alpha 5%, Error- beta 10% (P90%) we need 23 women in each group. Assuming a loss of 10% in the follow-up, the final size would be 52 women, 26 per group.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 92
• Est. completion date: June 1, 2019
• Est. primary completion date: March 1, 2019
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Vaginal delivery

• Cephalic presentation

• Primiparity

• At term gestation (37-42 weeks)

• No prior pelvic floor corrective surgery

• Written informed consent

Exclusion Criteria:

• Pregnancies with severe maternal or fetal pathology

Related Conditions & MeSH terms

• Disease
• Obstetric Trauma
• Pelvic Floor Disorders
• Physical Activity
• Physical Disorder

Intervention

Other:
• Physiotherapy treatment
Physiotherapy treatment consisted of pelvic floor exercises assisted by manometric biofeedback. In addition, active lumbopelvic stabilization exercises, including the contraction of pelvic floor muscles was performed in supine, plank and quadruped position.

Locations

Country	Name	City	State
Spain	Hospital Nuestra Señora de Valme	Sevilla

Sponsors (1)

Lead Sponsor	Collaborator
Hospital Universitario de Valme

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To evaluate the changes in pressure in the contractility evaluated by manometry (mm Hg)	To evaluate the changes in pressure in the contractility evaluated by manometry (mm Hg), of the medical floor produced by the treatment of postpartum physiotherapy of the pelvic floor	6 months after randomisation
Primary	Changes in muscle thickness (millimeters) of the levator ani muscle	Changes in muscle thickness (millimeters) of the levator ani muscle, measured with transperineal ultrasound 3-4D	6 months after randomisation