search
Back to results

Conservative Versus Surgical Treatment of Umbilical Pilonidal Disease

Primary Purpose

Pilonidal Sinus, Sinus; Dermal, Pilonidal, Umbilical Granuloma

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Surgery
conservative
Sponsored by
Medical Park Gaziantep Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pilonidal Sinus focused on measuring Umbilical pilonidal sinus, Treatment, Surgery, Conservative, Investigational treatment, After care

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • all patients willing to participate to the study with the diagnosis of umbilical pilonidal sinus

Exclusion Criteria:

  • no informed consent
  • serious coagulation abnormalities
  • known allergy to local anesthetics
  • pregnancy, or women who refused contraception at the time of treatment
  • other concomitant umbilical pathologies such as umbilical hernia, granuloma, dermoid cyst
  • the patients who diagnosed with urachal and omphalomesenteric anomalies through radiological investigation
  • patients who underwent umbilical operation

Sites / Locations

  • Hatem Hospital
  • Medical Park Gaziantep Hospital
  • 25 Aralık Familiy Physician Health Center
  • Dr.Ersin Arslan State Hospital
  • Şehitkamil State Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Surgery

Conservative

Arm Description

Circular incision 2-3 mm below the skin level in the umbilicus through the subcutaneous fat towards the linea alba. Dissection of the subcutaneous tissue within the umbilicus and its deep connection to preperitoneal fat through the linea alba. Excision of the umbilical complex containing pilonidal cyst 3 mm below the umbilical ostium. Approximation of the subcutaneous tissue with a single purse-string absorbable suture. The specimen, including the umbilical complex (pilonidal cyst, and involved skin and subcutaneous tissue), was transferred to department of pathology for histopathological examination.

Conservative treatment described as follow: Under local anesthesia, extracting all protruding hair, and curetting the granulation tissue and pilonidal cyst deep in the umbilicus. postoperative management include antibiotic treatment with ampicilline plus sulbactam and ornidazole, shaving surrounding skin, washing twice daily, and keeping umbilicus dry.

Outcomes

Primary Outcome Measures

Cure Rate
Primary outcome was the cure rate. Absence of recurrence within two year after the first treatment was considered as a cure. Recurrence was defined as the appearance of a new, active discharging sinus or granulation tissue with/without a bit of hairs in the deep of the umbilicus within two years after therapy.

Secondary Outcome Measures

Healing Time
the time form initial treatment to healing the wound and/or sinus and/or granulation tissue and no any sign of drainage with no longer need for dressing and wound care in either treatment arms.
Visual Analogue Scale for Patient Satisfaction (VAS-PS)
Well-being and satisfaction scales comprised linear metric scales known as "visual analogue scales," with grades from 0 (worst imaginable health state and extremely dissatisfied with the treatment) to 100 (best imaginable health state and extremely satisfied with the treatment).

Full Information

First Posted
August 8, 2012
Last Updated
December 23, 2016
Sponsor
Medical Park Gaziantep Hospital
Collaborators
Zeugma Saglik Hizmetleri San. Tic. Ltd. Sti.
search

1. Study Identification

Unique Protocol Identification Number
NCT01662765
Brief Title
Conservative Versus Surgical Treatment of Umbilical Pilonidal Disease
Official Title
Conservative Versus Surgical Treatment of Umbilical Pilonidal Sinus Disease: A Prospective, Randomised, and Multicenter Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
November 2003 (undefined)
Primary Completion Date
May 2010 (Actual)
Study Completion Date
May 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical Park Gaziantep Hospital
Collaborators
Zeugma Saglik Hizmetleri San. Tic. Ltd. Sti.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the study was to compare the results of conservative and surgical treatment, to create an algorithm for the management of the disease, and gain more information about the etiology, pathogenesis, and course of the disease. The investigators hypothesise that surgical treatment of UPS will be better than conservative management in terms of recurrence rate, healing time, patient comfort and satisfaction, and cost effectiveness.
Detailed Description
Because of its rarity, umbilical pilonidal sinus (UPS) is still poorly understood in terms of diagnosis, etiology, and the best treatment options. UPS is thought caused by hair penetrating the skin, leading to a foreign-body reaction and development of a sinus lined with granulation tissue. Most of the patients complain of pain, discharge or bleeding from the umbilicus when symptoms develop. It can be diagnosed with a careful examination, in which hairs can be seen deep in the umbilicus and usually protrude from a small sinus. Regarding the optimal treatment of the disease, a complete consensus has not yet been achieved. Some publications are recommended conservative treatment, while surgical treatment is recommended in others. A more meaningful comparison of the two modalities is that of a randomized controlled trial. We, therefore, present our data of prospective randomized controlled clinical trial comparing conservative versus surgical treatment of UPS. This was a multicenter, prospective balanced randomization, double blind, active-controlled, parallel-group, superiority study conducted in Turkey, under the direction of a principal investigator (MK). Eligible patients with UPS were randomized for either conservative treatment (CT) or surgical treatment (ST), and then the results of both groups were compared.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pilonidal Sinus, Sinus; Dermal, Pilonidal, Umbilical Granuloma
Keywords
Umbilical pilonidal sinus, Treatment, Surgery, Conservative, Investigational treatment, After care

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
84 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Surgery
Arm Type
Experimental
Arm Description
Circular incision 2-3 mm below the skin level in the umbilicus through the subcutaneous fat towards the linea alba. Dissection of the subcutaneous tissue within the umbilicus and its deep connection to preperitoneal fat through the linea alba. Excision of the umbilical complex containing pilonidal cyst 3 mm below the umbilical ostium. Approximation of the subcutaneous tissue with a single purse-string absorbable suture. The specimen, including the umbilical complex (pilonidal cyst, and involved skin and subcutaneous tissue), was transferred to department of pathology for histopathological examination.
Arm Title
Conservative
Arm Type
Active Comparator
Arm Description
Conservative treatment described as follow: Under local anesthesia, extracting all protruding hair, and curetting the granulation tissue and pilonidal cyst deep in the umbilicus. postoperative management include antibiotic treatment with ampicilline plus sulbactam and ornidazole, shaving surrounding skin, washing twice daily, and keeping umbilicus dry.
Intervention Type
Procedure
Intervention Name(s)
Surgery
Other Intervention Name(s)
umbilectomy
Intervention Description
modified umbilectomy
Intervention Type
Other
Intervention Name(s)
conservative
Other Intervention Name(s)
non-surgical management
Intervention Description
this treatment will include conservative procedures under local anesthesia for patient comfort.
Primary Outcome Measure Information:
Title
Cure Rate
Description
Primary outcome was the cure rate. Absence of recurrence within two year after the first treatment was considered as a cure. Recurrence was defined as the appearance of a new, active discharging sinus or granulation tissue with/without a bit of hairs in the deep of the umbilicus within two years after therapy.
Time Frame
2 year after initial treatment
Secondary Outcome Measure Information:
Title
Healing Time
Description
the time form initial treatment to healing the wound and/or sinus and/or granulation tissue and no any sign of drainage with no longer need for dressing and wound care in either treatment arms.
Time Frame
two year
Title
Visual Analogue Scale for Patient Satisfaction (VAS-PS)
Description
Well-being and satisfaction scales comprised linear metric scales known as "visual analogue scales," with grades from 0 (worst imaginable health state and extremely dissatisfied with the treatment) to 100 (best imaginable health state and extremely satisfied with the treatment).
Time Frame
30 days
Other Pre-specified Outcome Measures:
Title
Costs
Description
from initial treatment to the complete healing, all kind of cost will be calculated.
Time Frame
two year

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: all patients willing to participate to the study with the diagnosis of umbilical pilonidal sinus Exclusion Criteria: no informed consent serious coagulation abnormalities known allergy to local anesthetics pregnancy, or women who refused contraception at the time of treatment other concomitant umbilical pathologies such as umbilical hernia, granuloma, dermoid cyst the patients who diagnosed with urachal and omphalomesenteric anomalies through radiological investigation patients who underwent umbilical operation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mehmet KAPLAN, MD
Organizational Affiliation
Medical Park Gaziantep Hospital, Gaziantep, Turkey
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hatem Hospital
City
Gaziantep
ZIP/Postal Code
27090
Country
Turkey
Facility Name
Medical Park Gaziantep Hospital
City
Gaziantep
ZIP/Postal Code
27090
Country
Turkey
Facility Name
25 Aralık Familiy Physician Health Center
City
Gaziantep
ZIP/Postal Code
27100
Country
Turkey
Facility Name
Dr.Ersin Arslan State Hospital
City
Gaziantep
ZIP/Postal Code
27100
Country
Turkey
Facility Name
Şehitkamil State Hospital
City
Gaziantep
ZIP/Postal Code
27100
Country
Turkey

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27016906
Citation
Kaplan M, Ozcan O, Kaplan FC, Yalcin HC, Salman B. Conservative vs Surgical Interventions for Umbilical Pilonidal Sinus: A Multicenter, Double-Blind, Prospective, Randomized Clinical Trial. J Am Coll Surg. 2016 May;222(5):878-89. doi: 10.1016/j.jamcollsurg.2016.01.056. Epub 2016 Feb 23.
Results Reference
derived
Links:
URL
http://www.medicalpark.com.tr
Description
main study center

Learn more about this trial

Conservative Versus Surgical Treatment of Umbilical Pilonidal Disease

We'll reach out to this number within 24 hrs