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Function Following Laser for Anal Intraepithelial Neoplasia (FLAN)

Function Following Laser for Anal Intraepithelial Neoplasia (FLAN)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04109573
Acronym
FLAN
Enrollment
20
Registered
2019-09-30
Start date
2018-03-01
Completion date
2022-12-31
Last updated
2021-08-31

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

Conditions

Anal Intraepithelial Neoplasia, Anus Cancer, Fecal Incontinence, Post Operative Pain

Keywords

laser ablation, anal intraepithelial neoplasia, AIN, fecal incontinence, anal function

Brief summary

High-grade squamous intraepithelial lesions (HSIL) and anal cancer are rising in incidence and at highest risk are HIV positive men who have sex with men (MSM). This pilot study assessing anal function and patient-reported outcomes before and after laser ablation of HSIL will add to the evidence that such a therapy is an acceptable and safe treatment to offer in a preventative setting.We will be recruting HIV positive and negative MSM.

Detailed description

High resolution anoscopy with targeted laser ablation is one of the therapies currently employed to treat HSIL of the anus to prevent progression to anal cancer. The functional outcome of this procedure has not previously been formally assessed. HIV and negative positive MSM in whom HSIL has been detected will form the study population, as HSIL is prevalent in these patients and intervention is felt to be indicated. Functional assessments will be carried out prior to initial treatment and then repeated six months after laser ablation therapy. The structure, function and sensitivity of the anal canal will be evaluated using endoanal ultrasound, high-resolution anal manometry and anal mucosal electrosensitivity measurements respectively. Patient-reported outcomes will be assessed using questionnaires and semi-structured interviews at baseline, 4 weeks and 6 months post-treatment.

Interventions

PROCEDUREhigh resolution anal manometry

functional studies before and after anal laser ablation

Sponsors

Barts & The London NHS Trust
CollaboratorOTHER
Homerton University Hospital NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

MSM \>18 years of age if HIV positive, CD4 count of over 350; if less, been on highly active antiretroviral treatment for at least 3 months Histologically proven high-grade squamous anal intraepithelial neoplasia lesion (HSIL) Anal canal disease with or without perianal disease Written informed consent

Exclusion criteria

Previous laser or other ablative treatment for HSIL (previous topical treatment is not excluded) Any treatment for HSIL in the previous six months Previous or current diagnosis of anal cancer Concurrent or previous (if severe) perianal inflammatory bowel disease, complex fistula or other significant perianal condition requiring surgery including fissures, current fistula in ano and Grade III or IV haemorrhoids Perianal sepsis Perianal disease only without anal canal HSIL

Design outcomes

Primary

MeasureTime frameDescription
Manometric indicesSix monthsChanges in pressure vailues - resting pressure and maximum squeeze pressure compared to patient's own pre treatment values

Secondary

MeasureTime frameDescription
Anal mucosal sensitivity6 monthsChanges in sensitivity as measured against patients own pre treatment perception
Endoanal ultrasound abnormalities6 monthsChanges in endoanal ultrasound abnormalities compared to pre-treatment findings
Physical and psychological well-being4 weeks 6 monthsQualitative subjective physical and psychological well-being 4 weeks and 6 months after procedure of laser mucosal ablation of AIN
Patient reported outcomes6 monthsPatient reported outcomes, particularly with regard to sexual function and bowel function

Countries

United Kingdom

Contacts

Primary ContactTamzin Cuming, FRCS
Tamzin.cuming@nhs.net02085105555
Backup ContactChristine Inwang, MSc
christine.mitchell-inwang@nhs.net02085105134

Outcome results

None listed

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