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.
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
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:
- Pain after defecation lasting for more than three months;
- presence of a sentinel anal tag; and
- 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.
- Conditions
- Chronic Anal Fissure
- 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 group | Role | What they receive |
|---|---|---|
| Diltiazem, calcium channel blocker | Active comparator | Diltiazem gel 2% applied twice daily for 8 weeks Receives: Drug: Diltiazem |
| Levorag, Hibiscus plant extract | Experimental | Levorag 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.
Complete healing at week 12
Complete healing of the anal fissure after 12 weeks
Measured: 12 weeks
Secondary outcomes (4)
Complete healing at week 8
Complete healing of the anal fissure after 8 weeks
Measured: 8 weeks
Defecation pain at day 3
Perianal pain at or after defecation at day 3
Measured: 3 days
Defecation pain at day 7
Perianal pain at or after defecation at day 7
Measured: 7 days
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.
- First posted6 Jun 2014 (estimated)
- Study start1 Sep 2014
- Primary completion5 Feb 2018
- Study completion5 Feb 2018
Why it stopped: Slow inclusion rate
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Chronic Anal FissureStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Bispebjerg Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Sacomed
- Responsible party
- Principal investigator, Peter-Martin Krarup, Bispebjerg Hospital
- Investigators
- Peter-Martin Krarup, MD, Study chair, Bispebjerg HospitalAndreas Nordholm-Carstensen, MD, Principal investigator, Bispebjerg Hospital
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
Study at a glance
From the registry record, last updated by the sponsor on 14 Jan 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Treatment Of Chronic Anal Fissure (TOCA): a Randomized Clinical Trial on Levorag® Emulgel Versus Diltiazem Gel 2%
- ClinicalTrials.gov ID
- NCT02158013
- Acronym / sponsor ID
- TOCA / H-6-2014-020
- Conditions
- Chronic Anal Fissure
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Slow inclusion rate
- Enrolment
- 55 participants (actual)
- Lead sponsor
- Bispebjerg HospitalUniversity, hospital or other
- Collaborators
- Sacomed
- Study start
- 1 Sep 2014 (actual)
- Primary completion
- 5 Feb 2018 (actual)
- Study completion
- 5 Feb 2018 (actual)
- First posted
- 6 Jun 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to investigate the effect of Levorag Emulgel compared with diltiazem gel on the healing of chronic anal fissures.
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:
- Pain after defecation lasting for more than three months;
- presence of a sentinel anal tag; and
- 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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Diltiazem, calcium channel blocker | Active comparator | Drug: DiltiazemDiltiazem gel 2% applied twice daily for 8 weeks |
| Levorag, Hibiscus plant extract | Experimental | Other: Levorag EmulgelLevorag Emulgel applied twice daily for 8 weeks |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (8 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Levorag EmulgelAlso: Myoxinol, Carboxymethyl glucan | Other | Levorag, Hibiscus plant extract |
| Diltiazem | Drug | Diltiazem, calcium channel blocker |
Primary outcome
Complete healing at week 12
Time frame: 12 weeks
Complete healing of the anal fissure after 12 weeks
4 secondary outcomes
Complete healing at week 8
Time frame: 8 weeks
Defecation pain at day 3
Time frame: 3 days
Defecation pain at day 7
Time frame: 7 days
Adverse events
Time frame: 12 weeks
Results and safety
The study was stopped early (reason given: Slow inclusion rate). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Jan 2020.
- Derived from this study: PubMed 31980871Nordholm-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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Peter-Martin Krarup, MD study chair
Bispebjerg Hospital
Andreas Nordholm-Carstensen, MD principal investigator
Bispebjerg Hospital
2 sites in 1 country: see every site and its status.
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.