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Clinical Trials/NCT05717114
NCT05717114
Completed
Not Applicable

Efficacy of Different Doses of Dexmetomedine as an Adjuvant to Bupivacaine in Ultrasound Guided PECS Block in Patients Undergoing Modified Radical Mastectomy

Menoufia University1 site in 1 country96 target enrollmentFebruary 5, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post Operative Pain
Sponsor
Menoufia University
Enrollment
96
Locations
1
Primary Endpoint
postoperative pain
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Regional anesthesia is an essential component of anesthesia and analgesia. It has many advantages, it decreases pain post operatively, improves patient outcome and allow early recovery and ambulation Post-operative pain following breast surgery results from injured muscles and nerves, management of acute post operative pain is a consistent factor for better outcome and patient satisfaction

Detailed Description

All patients will be monitored by standard intraoperative monitoring that includes continuous electrocardiography (ECG), capnography, pulse oximetry, and non invasive blood pressure. Induction of general anesthesia will be done by propofol 1.5-2 mg/kg and fentanyl 3µg/kg. Tracheal intubation will be facilitated by administration of rocuronium 0.8 mg/kg. Anesthesia will be maintained with isoflurane 1MAC (Pecs block):the block will be performed with the patients in the supine position.The infraclavicular and axillary regions will be cleaned with antiseptic solution. the in plane technique will be used from proximal and medial to distal and lateral in an oblique manner at dermatome level T2 and T3.The puncture site was infiltrated with 2%lidocaine and once the structures is identified with Ultrasound

Registry
clinicaltrials.gov
Start Date
February 5, 2023
End Date
January 1, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

rabab Mohammad habeeb

Principal investigator

Menoufia University

Eligibility Criteria

Inclusion Criteria

  • adult patients
  • aged 18-60years old
  • ASA class 1 to 3
  • scheduled for elective modified radical mastectomy

Exclusion Criteria

  • patients refusal,
  • coagulopathies
  • concurrent anticoagulant therapy
  • allergy to local anaesthetics
  • infection at puncture site

Outcomes

Primary Outcomes

postoperative pain

Time Frame: 48 hours

Visual analog score for pain where 0 no pain and 10 most severe pain

Secondary Outcomes

  • Total morphine consumption(48 hours)

Study Sites (1)

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