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Clinical Trials/NCT06078241
NCT06078241CompletedNot Applicable

Intravenous Lidocaine Infusion Versus Ultrasound Guided Erector Spinae Plane Block for Postoperative Analgesia in Patients Undergoing Percutaneous Nephrolithotomy

Ain Shams University1 site in 1 country150 target enrollmentStarted: November 1, 2023Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
150
Locations
1
Primary Endpoint
Time to first rescue analgesia

Study Overview

Brief Summary

Percutaneous nephrolithotomy (PCNL) is a minimally invasive procedure to remove stones from the kidney by a small puncture wound through the skin. Patients receiving lidocaine infusion had lower pain scores, reduced postoperative analgesic requirements and decreased intraoperative anesthetic requirements. Erector spinae plane block (ESPB) seems to be effective when compared with no block or a placebo block.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Care Provider)

Eligibility Criteria

Ages
21 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • American Society of Anesthesiologists (ASA) score I-II..
  • Body mass index < 35 kg/m2.

Exclusion Criteria

  • Patient's refusal.
  • Known coagulopathy.
  • Known peripheral neuropathy or neurological deficits.
  • Chronic pain disorders.
  • Known allergy to study drugs

Arms & Interventions

Intravenous lidocaine infusion

Active Comparator

Intervention: Intravenous lidocaine infusion (Drug)

Erector spinae plane block (ESPB)

Active Comparator

Intervention: Erector spinae plane block (ESPB) (Other)

Intravenous infusion of normal saline and ESPB with normal saline

Placebo Comparator

Intervention: Intravenous infusion of normal saline (Other)

Intravenous infusion of normal saline and ESPB with normal saline

Placebo Comparator

Intervention: ESPB with normal saline (Other)

Outcomes

Primary Outcomes

Time to first rescue analgesia

Time Frame: 24 hours postoperatively

Time to first rescue analgesia

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ibrahim Mamdouh Esmat

Assistant Professor of Anesthesia and Intensive Care Department, Faculty of Medicine, Ain- shams University, Cairo, Egypt.

Ain Shams University

Study Sites (1)

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