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Pilonidal Sinus clinical trials

View clinical trials related to Pilonidal Sinus.

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NCT ID: NCT03764657 Completed - Pilonidal Sinus Clinical Trials

Pilonidal Sinus Disease: Preliminare Study

Start date: January 2017
Phase:
Study type: Observational [Patient Registry]

Pilonidal disease is morbid condition of young productive population, that could impair quality of life with high cost for health care system. No consensus exists on optimal surgical treatment, even if several techniques have been proposed. In this preliminary experimental case-control study the investigators compared excision by knife and diathermy with the aim to investigate if wound dehiscence could be related to heat spreading during excision of the sinus.

NCT ID: NCT03424057 Completed - Pilonidal Sinus Clinical Trials

Asymmetric Primary Closure and Additional Skin Excision Technique.

Start date: April 15, 2015
Phase: N/A
Study type: Interventional

The aim of this study was to reduce the residual dead-space volume with a modification following the standard Karydakis procedure.

NCT ID: NCT03070028 Completed - Pilonidal Sinus Clinical Trials

Minimally Invasive Treatment Methods for Pilonidal Disease

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT02849197 Completed - Pilonidal Sinus Clinical Trials

Study on Surgical Treatment of Pilonidal Sinus Disease

Start date: January 2011
Phase: N/A
Study type: Observational

Comparison of limited excision-primary closure, Limberg, and modified Limberg flap techniques for the surgical treatment of pilonidal sinus disease, each performed by a separate surgeon, in terms of postoperative outcomes and recurrence rates.

NCT ID: NCT02712970 Completed - Pilonidal Sinus Clinical Trials

Staging System for Chronic Symptomatic Pilonidal Sinus Disease

Start date: January 2011
Phase: N/A
Study type: Observational

A staging system was defined based on morphological extent of disease (stage I to stage IV for primary disease, and stage R for recurrent disease). Specific surgical technique was used for each stage. Demographics, perioperative data, short-term and long-term outcomes were evaluated according to the disease stage.

NCT ID: NCT02663466 Completed - Recurrence Clinical Trials

Off-midline Closure Errors as a Risk Factor for Recurrence Following Limberg Flap in Patients With Pilonidal Sinus

Start date: January 2015
Phase: N/A
Study type: Observational

Background. Limberg flap, one of the recently being popularized off-midline closure techniques, is widely performed for the treatment of sacrococcygeal pilonidal sinus; however, recurrences still can be seen. Objective. The aim of this study was to assess the relationship between recurrence and off-midline closure errors made in Limberg flap reconstructions. Design. A multicenter, matched-case-control study was conducted in three participating centers in Turkey. Settings. Each hospital's database was searched separately and all patients with and without recurrence who underwent LF surgery for primary SPS from January 2008 to July 2015 were identified. Patients. Sixty patients with recurrent disease (recurrent group, RG) and 120 matched cases of recurrence-free patients for at least 5 years following surgery (non-recurrent group, NRG) were included to the study. Interventions Main outcome measures. According to the off-midline closure concept, LF reconstructions were classified into incorrect closures (Type 1, 2 and 3) and correct closures (type 4, 5 and 6). Then the two groups were analyzed.

NCT ID: NCT02638064 Completed - Clinical trials for Pilonidal Sinus Disorder

Treatment of Pilonidal Sinus Disease Using Surgiflo as a Sealant: A New Concept

Start date: March 2013
Phase: N/A
Study type: Interventional

Assessment of surgiflo injection for treating pilonidal sinus disease

NCT ID: NCT02621879 Completed - Pilonidal Sinus Clinical Trials

Bilateral Gluteal Fascio-myo-cutaneous Flap in Treatment of Recurrent Pilonidal Disease

Start date: March 2012
Phase: N/A
Study type: Interventional

Bilateral Gluteal Fascio-myo-cutaneous Advancement Flap is a modified technique used in Treatment of Recurrent Sacrococcygeal Pilonidal sinus

NCT ID: NCT02574936 Completed - PILONIDAL SINUS Clinical Trials

Reduction Dead Space Volume With Karydakis Modification

Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to reduce the volume of dead space by a modification in kardakis flap procedure and consequently, to reduce the use of drains, wound drainage, seroma and hematoma formation, skin degradation and recurrence rates.

NCT ID: NCT02485860 Completed - Pilonidal Cysts Clinical Trials

Interest in the Use of Dressings With Honey for Wound Healing After Excision of Pilonidal Cyst

Pilomiel
Start date: March 8, 2016
Phase: Phase 4
Study type: Interventional

The management of pilonidal cysts is a skin excision and under deep skin. Scarring requires regular dressings (daily for 15 days and then every 48 hours) until complete healing. This healing is obtained on average in 68 days. Some patients have difficulties in healing with a final healing achieved on average in 95 days. Some teams use honey to promote wound cavitary wounds (wound infection, pressure ulcers, varicose wound). The acceleration of wound healing is due to antibacterial properties and hyperosmolarity to reduce secretions. ) The use of honey in pilonidal cysts is not evaluated and may accelerate healing.