Effect of Sacral Erector Spinae Plane Block on Hemorrhoid and Pilonidal Sinus Surgery

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06459739

Enrollment

Registered

2024-06-14

Start date

2023-09-01

Completion date

2024-04-01

Last updated

2025-02-27

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

Conditions

Anesthesia, Hemorrhoids, Pain, Acute Post-Operative, Pilonidal Sinus

Keywords

Sacral ESPB, Postoperative pain, Hemorrhoidectomy, Pilonidal sinus surgery, Analgesia

Brief summary

Introduction: This study investigated the efficacy of sacral erector spinae plane block (ESPB) for managing postoperative pain and reducing opioid consumption in patients undergoing hemorrhoid and pilonidal sinus (PS) surgery.

Detailed description

Interventions

PROCEDUREsacral ESPB

sacral ESPB

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 70 Years

Healthy volunteers

Inclusion criteria

* American Society of Anesthesiologists (ASA) I-II patients undergoing hemorrhoid and pilonidal sinus surgery

Exclusion criteria

* patients with coagulopathies, pregnant women, patients with significant cardiovascular, hepatic, or renal disease, patients who declined spinal anesthesia or were contraindicated for it, and patients who had previously undergone the same surgery

Design outcomes

Primary

Measure	Time frame	Description
Postoperative pain	0.5,2,8,24 hours	Numeric rating scale evaluation after surgery. Use 0 to 10 points with 0 no pain 5 moderate pain and 10 severe pain.

Secondary

Measure	Time frame	Description
Opioid consumption	0.5,2,8,24 hours	Admission of tramadol as a rescue analgesia

Countries

Turkey (Türkiye)

Outcome results

None listed

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