Treatment Of Chronic Anal Fissure
Information source: Bispebjerg Hospital
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Chronic Anal Fissure
Intervention: Levorag Emulgel (Other); Diltiazem (Drug)
Phase: N/A
Status: Recruiting
Sponsored by: Bispebjerg Hospital Official(s) and/or principal investigator(s): Peter-Martin Krarup, MD, Study Chair, Affiliation: Bispebjerg Hospital Andreas Nordholm-Carstensen, MD, Principal Investigator, Affiliation: Bispebjerg Hospital
Overall contact: Peter-Martin Krarup, MD, Phone: 004528732828, Email: TOCA.bispebjerg@gmail.com
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.
Clinical Details
Official title: Treatment Of Chronic Anal Fissure (TOCA): a Randomized Clinical Trial on Levorag® Emulgel Versus Diltiazem Gel 2%
Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: Complete healing at week 12
Secondary outcome: Complete healing at week 8Defecation pain at day 3 Defecation pain at day 7 Adverse events
Detailed 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 LevoragĀ® Emulgel, an ointment classified as Medical Device class 1.
According to the manufacturer (THD SpA, Italy) the effect of LevoragĀ® 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)
LevoragĀ® 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.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
1. Danish citizens, age ā„ 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
Locations and Contacts
Peter-Martin Krarup, MD, Phone: 004528732828, Email: TOCA.bispebjerg@gmail.com
Digestive Disease Center, Bispebjerg Hospital, Copenhagen DK2400, Denmark; Recruiting Tina Lee Broendum, Study Nurse, Phone: 004535313536, Email: Tina.Lee.Broendum@regionh.dk Peter-Martin Krarup, MD, Principal Investigator Andreas Nordholm-Carstensen, MD, Sub-Investigator
Additional Information
Starting date: September 2014
Last updated: July 20, 2015
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