Clinical Trials Directory

Trials / Completed

CompletedNCT03897933

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

Status
Completed
Phase
Study type
Observational
Enrollment
60 (actual)
Sponsor
TC Erciyes University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
PROCEDUREErector 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.
PROCEDUREnon- 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.

Timeline

Start date
2019-01-01
Primary completion
2020-01-01
Completion
2020-02-01
First posted
2019-04-01
Last updated
2022-08-01

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT03897933. Inclusion in this directory is not an endorsement.

Erector Spinae Plane Block for Postoperative Pain in Percutaneous Nephrolithotomy Patients: a Retrospective Study (NCT03897933) · Clinical Trials Directory