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Erector Spinae Plane Block for Postoperative Pain in Percutaneous Nephrolithotomy Patients: a Retrospective Study

NCT03897933 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2022-08-01

No results posted yet for this study

Summary

To evaluate the ability of Erector spina Plane block decrease postoperative pain and analgesia requirements in patients undergoing Percutaneous Nephrolithotomy.

Conditions

  • Percutaneous Nephrolithotomy

Interventions

PROCEDURE

Erector Spinae Plane block ( Group I)

ESP Block was performed preoperative to all patients in ESP block group. Patients in all groups were provided with intravenous patient- controlled analgesia device containing morphine for postoperative analgesia.

PROCEDURE

non- blocked Group (GROUP II)

This group was received no intervetion. Patients in all groups were provided with intravenous patient- controlled analgesia device containing morphine for postoperative analgesia.

Sponsors & Collaborators

  • TC Erciyes University

    lead OTHER

Principal Investigators

  • Sibel Pehlivan · TC Erciyes University

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-01
Primary Completion
2020-01-01
Completion
2020-02-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03897933 on ClinicalTrials.gov