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Clinical Trials/NCT04218149
NCT04218149
Completed
Phase 4

Comparison of the Effects of Serratus Plane Block and Erector Spinae Plane Block on Postoperative Analgesia in Patients Undergoing Unilateral Breast Surgery

Sisli Hamidiye Etfal Training and Research Hospital1 site in 1 country70 target enrollmentMay 1, 2019

Overview

Phase
Phase 4
Intervention
Bupivacaine Injection
Conditions
Breast Cancer
Sponsor
Sisli Hamidiye Etfal Training and Research Hospital
Enrollment
70
Locations
1
Primary Endpoint
Rescue analgesic
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Interfacial plan blocks are becoming more widely used for postoperative analgesia because of their easier applicability and less risk of complications. In this study, we aimed to compare the effects of serratus plane block (SPB) and erector spinae plane block (ESPB) on postoperative analgesia in patients undergoing unilateral breast surgery

Registry
clinicaltrials.gov
Start Date
May 1, 2019
End Date
October 1, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Sisli Hamidiye Etfal Training and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Kerim Şahin

research assistant

Sisli Hamidiye Etfal Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Age: 18 - 65 years
  • unilateral breast surgery

Exclusion Criteria

  • Does not approve the study
  • Emergency
  • ASA III-IV
  • History of local anesthetic allergy
  • Infection in the block area
  • Coagulation disorder
  • Morbid obesity (body mass index\> 40 kg / m²)
  • Severe organ failure
  • Previous neurological deficit
  • Psychiatric disease

Arms & Interventions

Group S

Serratus plane block with 25 ml %0.25 bupivacaine

Intervention: Bupivacaine Injection

Grup E

Erector spinae plane block with 25 ml %0.25 bupivacaine

Intervention: Bupivacaine Injection

Outcomes

Primary Outcomes

Rescue analgesic

Time Frame: Postoperative 24 hours

If VAS score is 4 or more, paracetamol 1 gr is administered

Postoperative pain score

Time Frame: Postoperative 24 hours

Visual analog scale (0-10), \<4 is adequate analgesia

Postoperative tramadol consumption

Time Frame: Postoperative 24 hours

Postoperative opiodi consumption with patient controlled analgesia

Secondary Outcomes

  • Analgesia time(Procedure)

Study Sites (1)

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