Evaluation of the Healing of the Pilonidal Cyst After 1940 nm Laser Treatment
PILOLAS 1940
1 other identifier
observational
30
1 country
1
Brief Summary
The aim of this study is to evaluate the extent to which the reduction of energy absorption that laser 1940 nm allows could improve the outcomes and postoperative results of the treatment of pilonidal cysts.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Oct 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 3, 2025
CompletedFirst Submitted
Initial submission to the registry
November 25, 2025
CompletedFirst Posted
Study publicly available on registry
December 8, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 30, 2026
December 8, 2025
November 1, 2025
9 months
November 25, 2025
November 25, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
HEALING
The main objective is to evaluate the healing rate of the pilonidal sinus one month after treatment with Er-YAG laser 1940 nm. Wound healing at one month, defined by the absence of a dressing, is the main evaluation criterion.
1 Month
Secondary Outcomes (1)
Recidivism
6 Month
Study Arms (1)
LASER 1940
Patient who underwent surgery for a pilonidal cyst using 1940 nm laser treatment
Interventions
Eligibility Criteria
patients treated with laser 1940 nm for a pilonidal cyst.
You may qualify if:
- Patients who did not object to the collection of their data
- Patients who underwent surgery for a pilonidal cyst using 1940 nm laser treatment
You may not qualify if:
- Patients with a history of pilonidal cyst surgery
- Patients who underwent emergency surgery for an abscess
- Patients already included in another therapeutic study protocol
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Clinique de la Sauvegarde
Lyon, 69009, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 25, 2025
First Posted
December 8, 2025
Study Start
October 3, 2025
Primary Completion (Estimated)
June 30, 2026
Study Completion (Estimated)
June 30, 2026
Last Updated
December 8, 2025
Record last verified: 2025-11