Anorectal Function in Perianal Crohn's Disease

Crohn Disease Clinical Trial

Official title:

Evaluation of Anorectal Function in Perianal Crohn's Disease: a Pilot Study.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03819257
• Other study ID #: GA18/113514
• Status: Completed
• Start date: January 19, 2019
• Est. completion date: February 22, 2020

Study information

• Verified date: February 2020
• Source: The Leeds Teaching Hospitals NHS Trust
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Perianal Crohn's disease is a disabling disease associated with increased morbidity and impaired quality of life. It is associated with pain, discharge, fecal incontinence and sexual and psychological impairment. In refractory cases, a stoma may be necessary. A higher prevalence is seen with increasing Crohn's disease duration and appears to vary according to the disease location. The presence of symptoms associated with anorectal dysfunction, such as fecal incontinence, can sometimes poorly correlate with the presence of anal sphincter abnormalities. Moreover, even in patients without symptoms, the presence of anal sphincter abnormalities may have important implications for the future selection of type of delivery, and might even pose a contra-indication for certain types of anorectal surgeries.

Studies evaluating possible chronic complications of perianal Crohn's disease on anorectal function are lacking. There is a need for a better understanding of the chronic complications of this disease, and the role of high-resolution anorectal manometry in diagnosing these abnormalities during follow-up of these patients. This study will evaluate the chronic repercussions of perianal Crohn's disease in patients with a previous anal fistula and/or abscess that has healed and/or is inactive.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: February 22, 2020
• Est. primary completion date: February 22, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. = 18 and = 75 year-old patients

2. CD in clinical remission, defined by a Harvey-Bradshaw index <5

3. Perianal CD history, defined by the presence of a perianal fistula and/or abscess that were treated/heal/inactive

4. Perianal Disease Activity Index (PDAI) of =4

5. Asymptomatic or symptomatic patients (anorectal symptoms) will be included, as long they fulfill the other inclusion criteria, like for anorectal symptomatic patients having a PDAI=4

6. Endoanal ultrasound without an image compatible with new/non-treated abscess or perianal fistula

7. Both previous simple or complex perianal fistula (according to the American College of Gastroenterology) will be considered.

Exclusion Criteria:

1. Women with previous vaginal delivery

2. Ileostomy

3. Previous anorectal surgery as hemorrhoidectomy or lateral sphincterotomy

4. Active rectal disease. No rectal involvement will be defined by no previous rectal involvement ever described or if previous involvement, endoscopy within 18 months showing no current involvement

5. Previous or current anal fissure

6. Anal stricture

7. Current or previous rectovaginal fistula (previous/last pelvic MRI).

A previous seton placement, abscess drainage, fistulotomy and lay open fistula are not an exclusion criteria. Patients with a current seton can only be included if the seton was place more than 24 weeks ago, and the endoanal ultrasound does not show any new/non-treated perianal fistula/abscess.

Related Conditions & MeSH terms

• Crohn Disease

Intervention

Diagnostic Test:
• Endoanal ultrasound
For the assessment of the internal and external anal sphincter integrity. To evaluate fistulas/perianal abscess and seton placement.
• High-resolution anorectal manometry
rest — basal anal pressures at rest over 60 s squeeze — anal pressure during voluntary effort; long squeeze — anal pressure during sustained voluntary effort cough — anorectal pressure changes during cough push — anorectal pressure changes during simulated defecation rectoanal inhibitory reflex — reflex anal response to rectal distension rectal sensation — assessment of rectal sensitivity to distension.
• Balloon expulsion test
A non-latex balloon will be inserted in the rectum after applying lubricating gel. This balloon is then filled with 50ml of warm water. The patient is ask to sit on a commode and to try to expel the device in privacy, while the time is being recorded. The test ends when the patient expelled the balloon or when 3 minutes are reach.

Locations

Country	Name	City	State
United Kingdom	Leeds Teaching Hospital NHS Trust	Leeds

Sponsors (1)

Lead Sponsor	Collaborator
The Leeds Teaching Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Wexner score (fecal incontinence score).	5 items score, including solid, liquid, gas incontinence, wearing pads and lifestyle alterations, scored from 0 (normal) to 4 (more severe).	5 minutes
Primary	Resting pressure, squeezing pressure, anorectal pressure changes during cough, anorectal pressure changes during simulated defecation, presence of a rectoanal inhibitory reflex and assessment of rectal sensitivity to distension.	Evaluated by high-resolution anorectal manometry.	30 minutes
Primary	Anal sphincters integrity.	Evaluated by endoanal ultrasound.	5 minutes
Primary	Ballon expulsion test duration.		3 minutes
Secondary	Presence of symptoms suggesting obstructed defection.	Prolonged and unsuccessful straining at stool, self-digitation for defecation, sense of incomplete evacuation or sensation of anorectal obstruction/blockage and a stool frequency of less than three times per week.	5 minutes