CArE for OAsI Study: Care Pathways and Anorectal Evaluation for OASI Associated Incontinence

Recruiting Observational Study
Obstetric Anal Sphincter Injury Severe Perineal Trauma Grade 3 Perineal Tear Grade 4 Perineal Tear Anal Incontinence Faecal Incontinence Urgency Deferral Time Pathways Follow-up Review Endo-anal Ultrasound Urogynaecology Biofeedback
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 50
Sex
Female
Study type
Observational
Participants needed
112 (estimated)
Sponsor
London North West Healthcare NHS Trust · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
The aim of this study is to ascertain which pathways currently exist in relation to the follow up of patients with obstetric anal sphincter injury related incontinence. This is particularly important as afflicted individuals may not readily volunteer information about their symptoms and struggles and need to be safeguarded by the presence of robust care pathways that ensure adequate follow up and …
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Part 1 of Study Inclusion Criteria: * • Fertile women ≥ 18 years and ≤50 who have developed OASI related incontinence following a vaginal delivery in the preceding five years (N.B. the average age of menopause in the UK is 51) * Tertiary referrals to the specialist perineal clinic as well as pa…
Contacts

No contact information available.