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Pilonidal sinus surgery under local anesthesia

Comparison of pilonidal sinus surgery complications between two methods of local and general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201312031786N5
Enrollment
60
Registered
2014-05-15
Start date
2013-03-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Pilonidal sinos. Pilonidal cyst without abscess

Interventions

Intervention 1: Local infiltration anesthesia group(Interventional) 0n=30)received local anesthesia solution of 20ml:12ml lidocaine 2% , 1ml epinephrine 1/200000 , 6ml bupivacaine 0.5% , 50µg fentanyl
in sacrococcygeal region. Intervention 2: General anesthesia for patients in the GA group(Control) will be used with intravenous midazolam 0.02ml/kg and fentanyl 3µg/kg as premedication and for induct
Treatment - Drugs
Local infiltration anesthesia group(Interventional) 0n=30)received local anesthesia solution of 20ml:12ml lidocaine 2% , 1ml epinephrine 1/200000 , 6ml bupivacaine 0.5% , 50µg fentanyl (1ml)
in sacrococcygeal region.
General anesthesia for patients in the GA group(Control) will be used with intravenous midazolam 0.02ml/kg and fentanyl 3µg/kg as premedication and for induction from propofol 2mg/kg, atracuriom 0.5 m

Sponsors

Vice chancellor for research, Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: informed written consent; ASA class ?-??. Exclusion criteria: recurrent and acute pilonidal sinus; substance abuse; cardiac disease; diabetes mellitus; sensitivity to local anesthetics; sever obesity (BMI>35).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The amount of intraoperative bleeding. Timepoint: At the end of operation. Method of measurement: Questionnaire.;The amount of intraoperative bleeding. Timepoint: At 3, 6, 24, 48 and 72 hours after surgery. Method of measurement: Visual Analog Scale.

Secondary

MeasureTime frame
O2 saturation. Timepoint: At the recovery in minutes 1, 10, 20 and 30. Method of measurement: Questionnaire.;Operation time. Timepoint: At the end of operation. Method of measurement: Questionnaire.;Respiratory rate. Timepoint: At the recovery in minutes 1, 10, 20 and 30. Method of measurement: Questionnaire.;Blood pressure. Timepoint: At the recovery in minutes 1, 10, 20 and 30. Method of measurement: Questionnaire.;The amount and type of analgesic drugs prescribed. Timepoint: During hospitalization. Method of measurement: Questionnaire.;The duration of hospitalization. Timepoint: Hospitalization. Method of measurement: Questionnaire.;Wound infection. Timepoint: One week and one month after surgery. Method of measurement: Questionnaire.;Wound seroma. Timepoint: One week and one month after surgery. Method of measurement: Questionnaire.;Recurrence. Timepoint: One week and one month after surgery. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyed Mohamad Javad Heidari Yazdi

Mazandaran University of Medical Sciences

javadheidari46@yahoo.com+98 15 1227 5038

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 12, 2026