Clinical Trials Logo

Clinical Trial Summary

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.


Clinical Trial Description

The study was a pilot study of 80 patients. Excluding criteria were previous sinüs surgery, active infection, patients who did not accept the procedure and patients under age of 18. After excision of the sinüs volume was measured using a beaker. A flap extending across the cut (Karydakis) was prepared in medial edge of the wound, 1 cm deep and 2 to 3 cm to be towards the interior. Prepared flap was shifted to the medial and sutured to presacral fascia with vicryl 2/0. To reduce the volume of the dead space formed in the lateral, 5 mm skin was excised along the incision in the flap side. Skin was approximated with sutures in the form of intermittent, using 2/0 poliprolen. No drain used. All patients were discharged on postoperative day 1. Sutures were removed 2 weeks later. All patients for at least 6 months were followed for wound drainage, seroma and hematoma formation, separation of skin and and recurrence. ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02574936
Study type Interventional
Source Siverek Devlet Hastanesi
Contact
Status Completed
Phase N/A
Start date January 2014
Completion date September 2015

See also
  Status Clinical Trial Phase
Active, not recruiting NCT01963273 - Video Assisted Ablation of Pilonidal Sinus N/A
Completed NCT00716937 - Karydakis Procedure Versus Excision With Healing by Secondary Intention (EHSI) in Sacrococcygeal Pilonidal Sinus Phase 4
Completed NCT06459739 - Effect of Sacral Erector Spinae Plane Block on Hemorrhoid and Pilonidal Sinus Surgery N/A
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 NCT01662765 - Conservative Versus Surgical Treatment of Umbilical Pilonidal Disease 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
Recruiting NCT06391307 - The Role of Mesenchymal Stem Cell and Exosome in Treating Pilonidal Sinus Disease in Children N/A
Not yet recruiting NCT06286397 - Topical Anti-Androgens in Pilonidal Sinus Disease Phase 2
Not yet recruiting NCT06406621 - Laser Hair Depilation Darker Skin Pilonidal Disease N/A
Completed NCT03923621 - Pilonidal Excision Versus Endoscopic Surgery N/A