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Epidural and Spinal Anesthesia Techniques in Pilonidal Dermoid Sinus Surgeries

Epidural and Spinal Anesthesia Techniques in Pilonidal Dermoid Sinus Surgeries: Prospective Randomized Trials

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02580500
Enrollment
100
Registered
2015-10-20
Start date
2015-10-31
Completion date
2016-01-31
Last updated
2016-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sinus; Dermal, Pilonidal

Keywords

Epidural anesthesia, Spinal anesthesia, pilonidal dermoid sinus

Brief summary

Pilonidal dermoid cyst surgery under general anesthesia and regional anesthesia techniques is used.regional anesthesia techniques; spinal, epidural, spinal epidural (combined) and is the local anesthesia.In the investigators study, pilonidal dermoid cyst surgery in spinal and epidural anesthesia techniques activity, reliability will be compared to the side effects and complications. One hundred patients will be randomly assigned to either the pilonidal dermoid cyst under Spinal anaesthesia (50 patients)(Group 1) or pilonidal dermoid cyst under epidural anaesthesia (50 patients)(Group 2). Group 1 will be used in spinal catheter in spinal anesthesia procedures or Group 2 will be used epidural catheter in epidural anaesthesia procedures.All patients has symptomatic pilonidal dermoid cyst.

Detailed description

Pilonidal dermoid is a tubular skin defect which can be seen in both female and male patients between the ages of 12 to 80. Treatment alternatives includes surgical excision. During the surgical treatment local, general, spinal or epidural anesthesia could be applied. However, local anesthesia usually is not preferred due to the fact that pilonidal dermoid sinuses depth, width could not be determined precisely. General anesthesia also is not preferred due to the fact that difficulties arising from patient's positioning and positioning based potential lung related problems. In general, spinal anesthesia and epidural anesthesia is preferred for pilonidal dermoid sinus surgeries. In this study, the investigators will demonstrate advantages, disadvantages, complications, (sensory and motor block levels), and durations of spinal and epidural anesthesia and superiority of each on these subjects. Patients who are over 18 and have a America Society of Anesthesiologist (ASA) physical score of I and II will be included in the study. Patients who are pregnant, have a known allergic reactions to local anesthetic and have contraindications against spinal and epidural anesthetic will be excluded from the study. In this study the investigators separate the patients into 2 groups. Group1: pilonidal dermoid cyst under Spinal anaesthesia (50 patients).Group 1 will be used in spinal catheter in spinal anesthesia procedures ; Group2:pilonidal dermoid cyst under epidural anaesthesia (50 patient).Group 2 will be used epidural catheter in epidural anaesthesia procedures. All patients has symptomatic pilonidal dermoid cyst

Interventions

epidural anaesthesia application for spinal catheter will be used

PROCEDUREspinal catheter

spinal anesthesia application for spinal catheter will be used

Sponsors

Lütfiye Nuri Burat Government Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* America Society of Anesthesiologist (ASA) physical score of I and II * the men and women over the age of 18, pilonidal sinus disease

Exclusion criteria

* Pediatric patients * Pregnant women * Patients with bleeding disorder * Patients with spinal deformity

Design outcomes

Primary

MeasureTime frameDescription
sensory block duration(time:hour)up to 6 hoursgroup1 and group 2

Secondary

MeasureTime frameDescription
Duration of operation(time:hour)up to 2 hoursgroup1 and group 2
Headachefrom end of the operation to postoperative 3 daysgroup 1 and group 2(participants)
Nausea/Vomitingfrom end of the operation to postoperative 1 daygroup 1 and group 2(participants)
Urinary Retentionfrom end of the operation to postoperative 1 daygroup 1 and group 2 (participants)

Countries

Turkey (Türkiye)

Contacts

Primary ContactTurgut Donmez, Surgeon
surgeont73@hotmail.com905347400967
Backup ContactVuslat Muslu Erdem, anesthetist
vuslatmuslu@gmail.com905326354139

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026