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Comparison of Postoperative Analgesic Efficacy of the Erector Spina Plane Block and Quadratus Lumborum Block in Open Nephrectomy: a Prospective Randomized Clinical Study

Comparison of Erector Spina and Quadratus Lumborum in Open Nephrectomy

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05810571
Enrollment
60
Registered
2023-04-12
Start date
2024-10-24
Completion date
2027-01-03
Last updated
2024-10-26

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

Conditions

Renal Cell Carcinoma

Keywords

erector spina plane block, quadratus lumborum block, patient controlled analgesia, nephrectomy, analgesia

Brief summary

patients who will undergo elective open nephrectomy will be divided into three groups; the control (PCA), the erector spina plane block, and the quadratus lumborum block. After standard anesthesia induction and monitorization then Bispectral index monitoring will be applied to all patients. Anesthesia will be maintained using sevoflurane in a mixture of oxygen and air. Continuous remifentanil infusion will be used for analgesia. Then patient's numeric rating scales and morphine pca consumptions will be recorded for one day.

Detailed description

patients who will undergo elective open nephrectomy will be divided into three groups; the control (PCA), the erector spina plane block and the quadratus lumborum block. After standard anesthesia induction and monitorization then Bispectral index monitoring will be applied to all patients. Anesthesia will be maintained using sevoflurane in a mixture of oxygen and air. Continious remifentanil infusion will be used for analgesia. Then patient's numeric rating scales and morphine pca consumptions will be recorded for one day.

Interventions

PROCEDUREpreoperative remifentanil consumption

continuous remifentanil infusion will applied for peroperative analgesia

PROCEDUREpostopeartive controlled anlagesia with morphine

postoperative morphine patient controlled analgesia will be applied for postoperative analgesia

Sponsors

Kocaeli University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

participant will not know which block applied, and the outcome assessor of the postoperative analgesia will not know

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* ASA 1-3 * open nephrectomy elective patients * BMI\<35

Exclusion criteria

* ASA 4-5-6 * Laparoscopic nephrectomy * infection at the block side * coagulation disorder * BMI\>35

Design outcomes

Primary

MeasureTime frameDescription
postoperative morphine consumption24 hour postoperativelyamount of postoperative morphine use of the patient's

Secondary

MeasureTime frameDescription
peroperative remifentanil consumptions4 hour preoperativelyamount of remifentanil use of the patient's
numeric rating scale24 hour postoperativelynumeric rating scores of the patient's postoepartively

Countries

Turkey (Türkiye)

Contacts

Primary Contactzehra ipek Arslan AYDIN, Professor
zehraipek48@gmail.com00905325011339
Backup ContactZehra ipek Arslan, Professor
zehraipek48@gmail.com00905325011339

Outcome results

None listed

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