Treatment Of Chronic Anal Fissure

Chronic Anal Fissure Clinical Trial

— TOCA  

Official title:

Treatment Of Chronic Anal Fissure (TOCA): a Randomized Clinical Trial on Levorag® Emulgel Versus Diltiazem Gel 2%

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02158013
• Other study ID #: H-6-2014-020
• Status: Terminated
• Phase: N/A
• Start date: September 1, 2014
• Est. completion date: February 5, 2018

Study information

• Verified date: January 2020
• Source: Bispebjerg Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effect of Levorag Emulgel compared with diltiazem gel on the healing of chronic anal fissures.

Description:

Anal fissure is an ulcer-like, longitudinal tear in the anal canal, most commonly located in the dorsal or ventral midline, and distal to the dentate line. Anal fissures constitute a common medical problem that affects sexes equally. The initiation of the fissure is most likely caused by the passage of hard stools that traumatizes the anal canal. Patients suffer from anal pain lasting up to several hours after defecation and rectal bleeding.3 Most acute anal fissures heal spontaneously, but a proportion progress into chronic fissures with symptoms beyond 8-12 weeks. There is no strict definition of a chronic anal fissure, but previously the presence of two of the following three symptoms has been used:

1. Pain after defecation lasting for more than three months;

2. presence of a sentinel anal tag; and

3. Exposure of the horizontal fibres of the internal anal sphincter. The severe pain may be caused by a hypertonic contraction of the internal anal sphincter leading to ischemia. Treatment strategies have therefore aimed to relieve this hypertonia by surgical and non-operative approaches. Primary therapy is initiated with ointments such as Diltiazem and glyceryltrinitrat gels.

A novel approach is the Levorag® Emulgel, an ointment classified as Medical Device class 1. According to the manufacturer (THD SpA, Italy) the effect of Levorag® Emulgel is mediated through the effects of myoxinol, a plant extract from the Hibiscus plant with a botox-like effects on the anal sphincter and carboxymethyl glucan, a natural yeast polysaccharide with immune stimulating properties. The effect of the widely used Diltiazem gel, is mediated through diltiazem hydrochloride, a calcium channel blocker that decreases the anal sphincter pressure.

This is an interventional, randomized clinical trial including adult patients with chronic anal fissures referred directly to the Digestive Disease Center, Bispebjerg Hospital, University of Copenhagen, or referred to a private surgical practice in Copenhagen. Patients are randomized to 1) Diltiazem gel 2%, one application twice daily for 8 weeks, or 2) Levorag® Emulgel, one application twice daily for 8 weeks. In addition to the allocated treatment, all patients will be kept on standard care for anal fissure, including high-fibre diet proper hydration and laxatives.

The primary endpoint is the rate of complete healing after 12 weeks. Secondary endpoints are complete healing after 8 weeks, incidence of adverse effects and efficacy on pain relief.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 55
• Est. completion date: February 5, 2018
• Est. primary completion date: February 5, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Danish citizens, age = 18 years

2. Presence of a midline anal fissure, dorsal or ventral

3. Pain during and after defecation lasting for more than 8 weeks

4. Presence of a sentinel anal tag or hypertrophic papilla

5. Exposure of the horizontal fibres of the internal anal sphincter

1-3 has to be fulfilled for inclusion. Additionally 4 AND/OR 5 has to be present

Exclusion Criteria:

1. Inflammatory bowel disease, known venereal disease, immunodeficiency disease

2. Anal/perianal abscess

3. Anal or rectal surgery within 12 weeks

4. Pregnancy or breastfeeding females

5. History of migraine or chronic headache requiring treatment with analgetics

6. Any cardiovascular or cerebrovascular disease

7. Current use of calcium channel blockers in general or history of use of calcium channel blockers in the treatment of the fissure

8. Signs of other rectal diseases, fistula, infection including severe perianal eczema and tumours

Related Conditions & MeSH terms

• Chronic Anal Fissure
• Fissure in Ano

Intervention

Other:
• Levorag Emulgel

Drug:
• Diltiazem

Locations

Country	Name	City	State
Denmark	Department of Surgery P, Aarhus University Hospital	Aarhus
Denmark	Digestive Disease Center, Bispebjerg Hospital	Copenhagen

Sponsors (2)

Lead Sponsor	Collaborator
Bispebjerg Hospital	Sacomed

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Incontinence	Cleveland Clinic incontinence score	8 and 12 weeks
Other	Anal resting pressure	Anal resting and maximal pressure measured by anal manometry (Peritron)	8 and 12 weeks
Primary	Complete healing at week 12	Complete healing of the anal fissure after 12 weeks	12 weeks
Secondary	Complete healing at week 8	Complete healing of the anal fissure after 8 weeks	8 weeks
Secondary	Defecation pain at day 3	Perianal pain at or after defecation at day 3	3 days
Secondary	Defecation pain at day 7	Perianal pain at or after defecation at day 7	7 days
Secondary	Adverse events	Any adverse events recorded during the study period	12 weeks