Actively Recruiting
Impact of Early Physiotherapy on Pain, Quality of Life, Pelvic Floor Function, and Sexual Health Post-Episiotomy
Led by Brno University Hospital · Updated on 2025-02-05
250
Participants Needed
1
Research Sites
117 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Surgical incision of the perineum and the posterior vaginal wall during a vaginal delivery (episiotomy) is among the most common surgical procedures performed in obstetrics. On the condition of having been performed correctly and in certain situations, episiotomy can be beneficial for a mother in decreasing the risk of a serious perineum injury. The benefit for a foetus can lie in acceleration of the final stage of delivery in the event of acute foetal distress. Many adverse effects are however connected to episiotomy. The morbidity connected to episiotomy can affect physical, mental, and social well-being of women during immediate as well as long-term post-partum periods. Currently, there are no universal standards that would describe and recommend physiotherapy for women following episiotomy during the first days, weeks, and months after a delivery. Care about the wound and the resulting scar after giving birth with episiotomy is an important topic because clinical experience shows that scars in the perineal area can have negative effects on the function of the pelvic floor muscles, on perineum pains, sexual health, and on mental well-being of a woman. Treatment of women with perineal wounds therefore requires a multidisciplinary approach, in which doctors, physiotherapists, and other medical professionals should be aware of the impact of a perineal scar on the quality of woman's life. Treatment or perineal scars, external genitalia, and the pelvic floor together with a targeted education of women in individual care after their scars should be part of evidence-based practice.
CONDITIONS
Official Title
Impact of Early Physiotherapy on Pain, Quality of Life, Pelvic Floor Function, and Sexual Health Post-Episiotomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female aged 18 to 40
- Following an uncomplicated mediolateral episiotomy
- Primipara at term with cephalic occiput anterior fetal position
- Signed informed consent and understanding of the study protocol
You will not qualify if you...
- Premature birth before 37 weeks gestation
- Fetal presentation other than cephalic occiput anterior
- Vaginal extraction performed
- Associated vaginal rupture
- Injury of the anal sphincter
- Paravaginal hematoma immediately after birth before study inclusion
- Multiple sclerosis
- Serious neurological disorders
- Connective tissue diseases
- Chronic inflammatory bowel diseases
- Congenital developmental disorders of the external genitalia
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospital
Brno, Czechia, 62500
Actively Recruiting
Research Team
L
Lukáš Hruban, PhD
CONTACT
M
Marika Bajerová, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here