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Analgesic Efficacy of Erector Spinae Plane Block after Percutaneous Nephrolithotomy: A Prospective Randomized Controlled Clinical Trial

Analgesic Efficacy of Erector Spinae Plane Block after Percutaneous Nephrolithotomy: A Prospective Randomized Controlled Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017602
Enrollment
Unknown
Registered
2018-08-06
Start date
2017-09-02
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

postoperative pain control

Interventions

Group B:ESPB by injecting 30 ml bupivacaine 0.25%
Group C:ESPB by injecting 30 ml normal saline

Sponsors

Dr. Soliman Fakeeh Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were patients with American Society of Anesthesiologists (ASA) physical status Classes I and II, aged 18–65 years, and scheduled for first-stage unilateral PCNL to extract stones which are large, multiple, or resistant to shockwave lithotripsy from the upper ureter and the pelvicalyceal system.

Exclusion criteria

Exclusion criteria: The exclusion criteria included patients with psychological disorders, morbid obesity, hepatic or renal dysfunction, coagulation disorders, sepsis, history of chronic analgesic use, and history of allergy to local anesthetics.

Design outcomes

Primary

MeasureTime frame
Morphine consumption over 24h (mg);

Secondary

MeasureTime frame
The time to the first use of PCA;In the postoperative period, assessment for pain using NRS on;Sedation was assessed at 2, 6, 12, and 24 h using the Ramsay sedation scale;patients satisfaction was assessed using a 5-point scale (1: very bad; 2: bad; 3: good; 4: very good; 5: perfect).;Duration of surgery;

Countries

Saudi Arabia

Contacts

Public ContactAli Mohamed Ali Elnabtity

Zagazig University, Egypt

alielnabtity@yahoo.com+20 0596785103

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 26, 2026