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Patient Controlled Erector Spinae Block at VATS

NCT04121000 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2021-06-02

No results posted yet for this study

Summary

In this study our aim is to investigate the effects of continue erector spinae block on postoperative pain in patients who underwent thoracoscopic surgery.

Conditions

  • Postoperative Pain

Interventions

PROCEDURE

VIDEO ASSISTED THOTACOSOPIC SURGERY

VATS

Sponsors & Collaborators

  • Bulent Ecevit University

    lead OTHER

Principal Investigators

  • OZCAN PISKIN · Bulent Ecevit University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-06-25
Primary Completion
2020-11-01
Completion
2020-12-31

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 NCT04121000 on ClinicalTrials.gov