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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05717114
Other study ID # 1/2023,ANET2-1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 5, 2023
Est. completion date January 1, 2024

Study information

Verified date January 2024
Source Menoufia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


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


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date January 1, 2024
Est. primary completion date December 25, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 60 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Pecs block
(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 inplane technique will be used from proximal and medial to distal and lateral in an oblique manner at dermatome level T2and T3.The puncture site was infiltrated with 2%lidocaine and once the structures is identified with ultrasound.

Locations

Country Name City State
Egypt Menoufia Menoufia ????????

Sponsors (1)

Lead Sponsor Collaborator
Menoufia University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative pain Visual analog score for pain where 0 no pain and 10 most severe pain 48 hours
Secondary Total morphine consumption Mg 48 hours
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