Minimally Invasive Treatment Methods for Pilonidal Disease
Primary Purpose
Pilonidal Sinus
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
crystallised phenol
Platelet rich plasma
Sponsored by
About this trial
This is an interventional treatment trial for Pilonidal Sinus
Eligibility Criteria
Inclusion Criteria:
- Having pilonidal sinus disease
- accepting to be involved in the study
Exclusion Criteria:
- below the age of 18
- having connective tissue disorders
- diabetes mellitus
- severe anemia
Sites / Locations
- Uşak University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Phenol
platelet rich plasma
Arm Description
crystallised phenol application
PRP application
Outcomes
Primary Outcome Measures
healing time
Time to complete closure of the sinus cavity.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03070028
Brief Title
Minimally Invasive Treatment Methods for Pilonidal Disease
Official Title
Randomized Prospective Comparison of Crystallized Phenol and Platelet Rich Plasma Applications in Treatment of Pilonidal Sinus Disease
Study Type
Interventional
2. Study Status
Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
January 1, 2017 (Actual)
Primary Completion Date
December 1, 2019 (Actual)
Study Completion Date
May 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Uşak University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patients with pilonidal sinus disease will be randomised to two groups (crystallised phenol and platelet rich plasma). Sinus healing time, patient satisfaction, complications and recurrence rates will be compared.
Detailed Description
Patients with pilonidal sinus disease will be treated by either crystallised phenol or platelet rich plasma application. Treatment results, healing time, postprocedural complications, patient satisfaction and recurrences will be compared.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pilonidal Sinus
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
200 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Phenol
Arm Type
Experimental
Arm Description
crystallised phenol application
Arm Title
platelet rich plasma
Arm Type
Experimental
Arm Description
PRP application
Intervention Type
Procedure
Intervention Name(s)
crystallised phenol
Intervention Description
crystallised phenol will be applied to sinus cavity
Intervention Type
Procedure
Intervention Name(s)
Platelet rich plasma
Intervention Description
platelet rich plasma will be applied to sinus cavity
Primary Outcome Measure Information:
Title
healing time
Description
Time to complete closure of the sinus cavity.
Time Frame
first 1 year of the study
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Having pilonidal sinus disease
accepting to be involved in the study
Exclusion Criteria:
below the age of 18
having connective tissue disorders
diabetes mellitus
severe anemia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Barış Sevinç, M.D.
Organizational Affiliation
Uşak University Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
Uşak University
City
Uşak
ZIP/Postal Code
64100
Country
Turkey
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34629430
Citation
Sevinc B, Damburaci N, Karahan O. Comparison of Curettage Plus Platelet-Rich Plasma Gel and Curettage Plus Phenol Application in Treatment of Pilonidal Sinus Disease: A Randomized Trial. Dis Colon Rectum. 2022 May 1;65(5):735-741. doi: 10.1097/DCR.0000000000002082.
Results Reference
derived
Learn more about this trial
Minimally Invasive Treatment Methods for Pilonidal Disease
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