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

T

TC Erciyes University

Status

Completed

Conditions

Percutaneous Nephrolithotomy

Treatments

Procedure: non- blocked Group (GROUP II)
Procedure: Erector Spinae Plane block ( Group I)

Study type

Observational

Funder types

Other

Identifiers

NCT03897933
2019/881

Details and patient eligibility

About

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

Full description

Erector spina Plane block was performed with guided ultrasound at T10 Transverse process level would lead to adequate postoperative analgesia ,in Percutaneous Nephrolithotomy surgeries.

Enrollment

60 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA I- ASA II Patients

Exclusion criteria

  • history of allergy to the study medication
  • refusal to participate

Trial design

60 participants in 2 patient groups

Erector spinae plane block group (ESP)
Description:
Single- shot ultrasound guided ESP block with 30 ml 0.25% bupivacain at the T10 vertebral level was performed preoperatively to patients in the ESP group (Group I).
Treatment:
Procedure: Erector Spinae Plane block ( Group I)
non- blocked Group
Description:
consists of the patient group without any procedure
Treatment:
Procedure: non- blocked Group (GROUP II)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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