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Microbiota in Chronic Anal Fissure and Its Association With Prognosis

Microbiota in Chronic Anal Fissure and Its Association With Prognosis - Prospective Cohort Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05405634
Enrollment
80
Registered
2022-06-06
Start date
2022-09-30
Completion date
2023-06-30
Last updated
2022-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anal Fissure, Microbial Colonization

Brief summary

In this study, we will try to answer the following questions: 1. What are the salient features of the microbiota in chronic anal fissure? 2. Are these features associated with prognosis and response to therapy? 3. Does an anal fissure swab and anal fissure tissue give comparable bacteriological results?

Detailed description

To allow rational planning of therapeutic trials of antimicrobial or biofilm degrading medical therapy, a better understanding of the microbiota of chronic anal fissures is needed. Previous studies have relied on culture, whereas we will employ molecular methods. We will collect bacteriological samples from patients referred to us with anal fissure, in order to characterize the microbiota. To see if the microbiota is distinct from or similar to the rectal microbiota, we will also collect a swap from the rectum. We will also collect swaps from the anal verge of healthy volunteers without anal fissure, to see if the microbiota in anal fissures are distinct from the normal anodermal microbiota. To examine whether a swap is a reliable method for characterizing the microbiota in anal fissure, we will also collect excised anal fissure tissue from the subset of patients with a clinical indication for fissurectomy in general anaesthesia, and compare the analysis results with those from the swap. We will re-assess the patients clinically and with a repeat swap after 3 months, and perform an exploratory analysis in order to identify possible features of the microbiota that are associated with poor response to therapy.

Interventions

None listed

Sponsors

Lasse Krogsbøll
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Three samples will be included: 1. Consecutive patients referred to the outpatient clinic at the Digestive Disease Centre, Bispebjerg Hospital in Denmark for botox injection for chronic anal fissure. Thus, the included patients will likely all have tried conservative treatment before referral, and are expected to represent a more homogeneous subset with longer standing disease, less spontaneous improvement, and a higher likelihood of being compliant with suggested therapy 2. Consecutive patients with an indication for revision of the fissure and anal injection of botulinum toxin in general anaesthesia 3. Healthy volunteers. These will be recruited among staff at the Digestive Disease Centre, Bispebjerg Hospital, Denmark. Samples 1 and 2 will not be independent, as patients from group 1 may be included in group 2 depending on the clinical course. No direct comparisons between these two groups are planned (see analysis section).

Exclusion criteria

* Symptom duration of less than 8 weeks (groups 1 and 2) * Known or suspected Crohn's disease * Known or suspected active venereal disease.

Design outcomes

Primary

MeasureTime frameDescription
16S/18S RNABaseline
PICRUSt2Baseline
Healing of anal fissure after 3 months3 monthsDefined by complete patient-reported resolution of pain combined with healed fissure on clinical examination
Change from baseline in pain severity both during and after defecation3 monthsNumerical rating scale 1-10.

Contacts

Primary ContactLasse T Krogsbøll, MD, PhD
lasse.theis.krogsboell@regionh.dk0045 51684692
Backup ContactAndreas Nordholm-Carstensen, MD, PhD
andreas.nordholm-carstensen@regionh.dk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026