Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05810571

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
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Kocaeli University · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREpreoperative remifentanil consumptioncontinuous remifentanil infusion will applied for peroperative analgesia
PROCEDUREpostopeartive controlled anlagesia with morphinepostoperative morphine patient controlled analgesia will be applied for postoperative analgesia

Timeline

Start date
2024-10-24
Primary completion
2027-01-03
Completion
2027-01-03
First posted
2023-04-12
Last updated
2024-10-26

Locations

2 sites across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05810571. Inclusion in this directory is not an endorsement.