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.
At a Glance
- Age
- 18 – 50
- Sex
- Female
- Study type
- Observational
- Participants needed
- 112 (estimated)
- Sponsor
- London North West Healthcare NHS Trust · Other
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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
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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
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