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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01662765
Other study ID # MK-003-UPS
Secondary ID
Status Completed
Phase N/A
First received August 8, 2012
Last updated August 9, 2012
Start date November 2003
Est. completion date May 2012

Study information

Verified date August 2012
Source Medical Park Gaziantep Hospital
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Interventional

Clinical Trial Summary

The Investigator's information in the Responsible Party data elements is not properly formatted. Please provide the investigator's "Official Title" (e.g., Director, Head of Otolaryngology, Principal Investigator, Clinical Professor).Pilonidal sinus disease is a common health problem. It is seen most frequently in the sacrococcygeal region. However, it can also observed in the umbilicus. Although rare, umbilical pilonidal sinus (UPS) disease, is still poorly understood both in terms of diagnosis or pathophysiology and the best treatment options. The incidence and the prevelance of the disease is thought to be 0.6% and %0.1, respectively, and is more common in males.

Pilonidal sinus disease of the umbilicus is caused by hair penetrating the skin, causing 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.

The first article, which can be considered as umbilical pilonidal sinus disease was first published by Dr. Warren in 1854, and he described the removal of a sprinkle of hair from the umbilicus. But the term "umbilical pilonidal sinus" was first described and used by Williams and Patey in 1956. Since this initial reference to umbilical pilonidal sinus there have been approximately only 30 reports in the literature. Most of them are case reports and remaining consists of small case series. But until now no prospective randomised studies have been published related to UPS.

UPS is one of the most neclected disease that few reported studies and lack of the prospective randomised studies in the literature, and no cosensus about the treatment of the disease supports this idea. However, it may be actually more common than thought and may be found more frequently if sought specifically.

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 etiologiy, 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.


Recruitment information / eligibility

Status Completed
Enrollment 84
Est. completion date May 2012
Est. primary completion date May 2010
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility 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

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Intervention

Procedure:
Surgery
modified umbilectomy
Other:
conservative
this treatment will include conservative procedures under local anesthesia for patient comfort.

Locations

Country Name City State
Turkey 25 Aralik Familiy Physician Health Center Gaziantep
Turkey Dr.Ersin Arslan State Hospital Gaziantep
Turkey Hatem Hospital Gaziantep
Turkey Medical Park Gaziantep Hospital Gaziantep
Turkey Sehitkamil State Hospital Gaziantep

Sponsors (2)

Lead Sponsor Collaborator
Medical Park Gaziantep Hospital Zeugma Saglik Hizmetleri San. Tic. Ltd. Sti.

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other costs from initial treatment to the complete healing, all kind of cost will be calculated. two year No
Primary cure rate Primary outcome was the cure rate. Absence of recurrence within two year after the first treatment was considered as a cure. In contrast, a 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. 2 year after initial treatment No
Secondary 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. two year No
Secondary complications formation chronic non-healing wound, bleeding, and infection two years No
Secondary patient satisfaction it will evaluated in five categories as follow: very satisfied, satisfied, not bad, unsatisfied, worst two years No
See also
  Status Clinical Trial Phase
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Completed NCT00716937 - Karydakis Procedure Versus Excision With Healing by Secondary Intention (EHSI) in Sacrococcygeal Pilonidal Sinus Phase 4
Recruiting NCT05474911 - PILONIDAL SINUS: CONVENTIONAL CARE VERSUS NEGATIVE PRESSURE THERAPY. N/A
Completed NCT04599517 - The Most Frequently Preferred Surgical Method In The Treatment Of Sacrococcygeal Pilonidal Disease
Recruiting NCT02539693 - Sacrococcygeal Local Anesthesia With Different Doses of Clonidine for Pilonidal Sinus Surgery N/A
Completed NCT01081522 - A Preliminary, Non-comparative Study to Evaluate a Bioresorbable Wound Scaffold in Acute Wounds N/A
Completed NCT00997048 - Comparison Between Laying Open and Sinus Excision of Pilonidal Sinus - a Randomized Study N/A
Not yet recruiting NCT04273997 - Metronidazole Ointment in Non-healing Pilonidal Sinus Wounds Phase 2
Recruiting NCT06324656 - The Efficacy of Combining Platelet-rich Plasma With Crystallized Phenol in Pilonidal Sinus Disease N/A
Completed NCT02246192 - Use of Plasma Rich in Growth Factors (PRGF) in Pilonidal Sinus Excision N/A
Completed NCT06206330 - Effect of Platelet Rich Plasma (PRP) on Healing Time in Patients Following Pilonidal Sinus Surgery N/A
Recruiting NCT04217824 - Comparison of Karydakis and Limberg Flap Treatment of Pilonidal Sinus in Adolescent. a Prospective, Randomised Study N/A
Recruiting NCT03483480 - Non-Powered Negative Pressure Wound Therapy vs Open Technique for Pilonidal Disease N/A
Not yet recruiting NCT06140199 - Comparing Minimally Invasive Treatments for Pilonidal Disease: LA POPA Trial (Laser And Pit-picking OR Pit-picking Alone) N/A
Not yet recruiting NCT06286397 - Topical Anti-Androgens in Pilonidal Sinus Disease Phase 2
Completed NCT03923621 - Pilonidal Excision Versus Endoscopic Surgery N/A
Active, not recruiting NCT01792557 - Crystallized Phenol Versus Transposition Flaps for Treatment of Pilonidal Disease: A Prospective Study N/A
Completed NCT02621879 - Bilateral Gluteal Fascio-myo-cutaneous Flap in Treatment of Recurrent Pilonidal Disease N/A
Completed NCT00412659 - Mid-line Excision Versus Karydakis Operation for Pilonidal Sinus Phase 2/Phase 3
Completed NCT04697082 - Application of Platelet-rich Plasma in Pilonidal Sinus Disease N/A

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