Minimally Invasive Treatment Methods for Pilonidal Disease

NCT ID: NCT03070028

Last Updated: 2020-05-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-01-01

Study Completion Date

2020-05-01

Brief Summary

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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

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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.

Conditions

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Pilonidal Sinus

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Phenol

crystallised phenol application

Group Type EXPERIMENTAL

crystallised phenol

Intervention Type PROCEDURE

crystallised phenol will be applied to sinus cavity

platelet rich plasma

PRP application

Group Type EXPERIMENTAL

Platelet rich plasma

Intervention Type PROCEDURE

platelet rich plasma will be applied to sinus cavity

Interventions

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crystallised phenol

crystallised phenol will be applied to sinus cavity

Intervention Type PROCEDURE

Platelet rich plasma

platelet rich plasma will be applied to sinus cavity

Intervention Type PROCEDURE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Uşak University

OTHER

Sponsor Role lead

Responsible Party

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Barış Sevinç

assistant proffessor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Barış Sevinç, M.D.

Role: PRINCIPAL_INVESTIGATOR

Uşak University Medical School

Locations

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Uşak University

Uşak, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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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.

Reference Type DERIVED
PMID: 34629430 (View on PubMed)

Other Identifiers

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PS001

Identifier Type: -

Identifier Source: org_study_id

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