erector spinae plane block for analgesia in pilonidal sinus surgery

Role of ultrasound guided sacral erector spinae plane block for postoperative analgesia in pilonidal sinus surgery

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

PACTR

Registry ID

PACTR201912565389988

Enrollment

Registered

2019-12-17

Start date

2019-12-15

Completion date

Unknown

Last updated

2026-01-27

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

Conditions

Surgery Anaesthesia

Interventions

general anesthesia

sacral erector spinae plane block

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: seventy patients aged 20-60 years old both sex ASA class I and II eligible for pilonidal sinus surgery

Exclusion criteria

Exclusion criteria: patient's refusal pre-existing neurological or psychiatric illness mental retardation BMI >35 kg/m2 Allergy to local anesthetics Infection at the injection site

Design outcomes

Primary

Measure	Time frame
pain score	—

Secondary

Measure	Time frame
total fentanyl consumption;the time to first analgesic request;complications e.g. local anesthetic toxicity, nausea, or vomiting	—

Countries

Egypt

Contacts

Public ContactShimaa Elrahwan

lecturer

Shimaa.mostafa911@yahoo.com+201007186300

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Feb 4, 2026