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Chronic Anal FissureTOCANCT02158013

Treatment Of Chronic Anal Fissure

A study testing Levorag Emulgel and Diltiazem in people with Chronic Anal Fissure, run by Bispebjerg Hospital at 2 sites in Denmark.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Chronic Anal Fissure
What is being tested?
Levorag Emulgel and Diltiazem
Could I receive a placebo?
No, everyone receives an active treatment
How many people
55 participants
Where
2 sitesDenmark
Study dates
1 Sep 2014to 5 Feb 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Danish citizens, age ≥ 18 years
  • Presence of a midline anal fissure, dorsal or ventral
  • Pain during and after defecation lasting for more than 8 weeks
  • Presence of a sentinel anal tag or hypertrophic papilla
  • 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

Who cannot join

  • Inflammatory bowel disease, known venereal disease, immunodeficiency disease
  • Anal/perianal abscess
  • Anal or rectal surgery within 12 weeks
  • Pregnancy or breastfeeding females
  • History of migraine or chronic headache requiring treatment with analgetics
  • Any cardiovascular or cerebrovascular disease
  • Current use of calcium channel blockers in general or history of use of calcium channel blockers in the treatment of the fissure
  • Signs of other rectal diseases, fistula, infection including severe perianal eczema and tumours

Trial locations and contacts

2 sites in 1 country.

Denmark2 sites
  • Department of Surgery P, Aarhus University Hospital

    Aarhus, DK8000

  • Digestive Disease Center, Bispebjerg Hospital

    Copenhagen, DK2400

Other trials in Denmark

About this study

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

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

Read the 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 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.

Being tested
Levorag Emulgel, Diltiazem

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Levorag EmulgelOther

    Also called Myoxinol, Carboxymethyl glucan

  • DiltiazemDrug

Study groups in NCT02158013
Study groupRoleWhat they receive
Diltiazem, calcium channel blockerActive comparatorDiltiazem gel 2% applied twice daily for 8 weeks
Receives: Drug: Diltiazem
Levorag, Hibiscus plant extractExperimentalLevorag Emulgel applied twice daily for 8 weeks
Receives: Other: Levorag Emulgel

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Complete healing at week 12

    Complete healing of the anal fissure after 12 weeks

    Measured: 12 weeks

Secondary outcomes (4)
  1. Complete healing at week 8

    Complete healing of the anal fissure after 8 weeks

    Measured: 8 weeks

  2. Defecation pain at day 3

    Perianal pain at or after defecation at day 3

    Measured: 3 days

  3. Defecation pain at day 7

    Perianal pain at or after defecation at day 7

    Measured: 7 days

  4. Adverse events

    Any adverse events recorded during the study period

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Jun 2014 (estimated)
  2. Study start1 Sep 2014
  3. Primary completion5 Feb 2018
  4. Study completion5 Feb 2018

Why it stopped: Slow inclusion rate

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Care provider, Investigator, Outcomes assessor
Enrolment
55 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02158013
Sponsor's protocol ID
H-6-2014-020
Acronym
TOCA
Status last verified
Jan 2020
First submitted
5 Jun 2014
Last updated
14 Jan 2020
Results posted
No
Data monitoring committee
No

Publications

  • Nordholm-Carstensen A, Perregaard H, Wahlstrom KL, Hagen KB, Hougaard HT, Krarup PM. Treatment of chronic anal fissure: a feasibility study on Levorag(R) Emulgel versus Diltiazem gel 2. Int J Colorectal Dis. 2020 Apr;35(4):615-621. doi: 10.1007/s00384-020-03515-z. Epub 2020 Jan 24.

    PubMed 31980871

Questions about this trial

What is this clinical trial studying?

A study testing Levorag Emulgel and Diltiazem in people with Chronic Anal Fissure, run by Bispebjerg Hospital at 2 sites in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 14 Jan 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Slow inclusion rate). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Complete healing at week 12 (time frame: 12 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02158013, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jan 2020.

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