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Clinical Trials/NCT05911373
NCT05911373CompletedNot Applicable

Serratus Plane Block Versus Serratus Plane Block Plus Parasternal Block on Postoperative Opioid Consumption and Dermatomal Analyses for Breast Surgery

Ataturk University1 site in 1 country64 target enrollmentStarted: June 21, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
64
Locations
1
Primary Endpoint
Postoperative opioid consumption

Study Overview

Brief Summary

Mastectomy is a technique often used in breast cancer surgery. Patients experience moderate to severe pain postoperatively after this procedure. Various plane blocks, NSAIDs, and opioid analgesics can be administered to these patients as components of multimodal analgesia. In the the study, the investigators aimed to evaluate the analgesic effects of the serratus plane block, the parasternal block added to the serratus plane block, and the dermatomal differences.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •American Society of Anesthesiologist's physiologic state I-III patients
  • •To undergo Mastectomy Surgery
  • •Being between the ages of 18-65 years

Exclusion Criteria

  • •Having a known heart, kidney, liver or hematological disease
  • •Having a history of peptic ulcer, gastrointestinal bleeding, allergy, chronic pain
  • •Routine analgesic use and history of analgesic use in the last 24 hours
  • •Not willing to participate in the study
  • •Uncooperative patients who have coagulopathy or use anticoagulant drugs
  • •To be allergic to one of the drugs to be used

Arms & Interventions

group serratus

Placebo Comparator

preoperative superficial serratus block with local anaesthetics and parasternal block with saline

Intervention: group serratus plan block (Other)

group serratus and parasternal

Active Comparator

preoperative superficial serratus block and parasternal block with local anaesthetics

Intervention: group serratus and parasternal plan block (Other)

Outcomes

Primary Outcomes

Postoperative opioid consumption

Time Frame: first 24 hours

First 24 hours total fentanyl consumption with patient controlled analgesia

Secondary Outcomes

  • Sensory Assessment(24 hours)
  • Visual analog pain score(First 24 hours)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ali Ahiskalioglu

Principal Investigator

Ataturk University

Study Sites (1)

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