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Prospective Study in Laser Treatment of Pilonidal Cysts (LASPRO)

C

Centre Hospitalier Departemental Vendee

Status

Not yet enrolling

Conditions

Pilonidal Sinus

Study type

Observational

Funder types

Other

Identifiers

NCT07314632
2025-A02356-43 (Other Identifier)
CH25_0098

Details and patient eligibility

About

The goal of this observational study is to evaluate the recurrence rate after laser treatment of pilonidal sinus within two years of the procedure in adult patients who require this procedure to treat their pilonidal sinus.

The main question it aims to answer is:

• Is there a clinical recurrence (presence of a fistula in the intergluteal cleft) 2 years after laser treatment of pilonidal sinus? Participants who undergo surgery as part of their regular medical care will answer survey questions about recurrence at 1 and 2 years.

Enrollment

240 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients requiring laser surgery for pilonidal sinus, of any type (including recurrence after radical cure or laser treatment)
  • Patient able to understand the protocol and having given written informed consent to participate in the study,
  • Patient affiliated to the social security system or entitled to it.

Exclusion criteria

  • Patient participating in another interventional clinical research protocol involving a drug or clinical investigation of a medical device
  • Patient already included in a research study
  • Patient under guardianship, conservatorship, or deprived of liberty
  • Patient under an activated future protection mandate
  • Patient under family authorization
  • Patient under judicial protection.

Trial design

240 participants in 1 patient group

Patients requiring laser surgery for pilonidal sinus
Description:
pilonidal sinus of any type (including recurrence after radical cure or laser treatment)

Trial contacts and locations

2

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Central trial contact

Agnès DORION

Data sourced from clinicaltrials.gov

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