Efficacy of Serratus Anterior Plane Block Mastectomy
- Conditions
- Postoperative ComplicationsPostoperative Pain
- Interventions
- Procedure: serratus anterior plan block
- Registration Number
- NCT03944759
- Lead Sponsor
- doaa rashwan
- Brief Summary
Breast cancer is the main common cancer among females. . Inadequate control of pain may later develop into chronic pain syndrome (paraesthesias, phantom breast pain, and intercostobrachial neuralgia) in 25-40% of the patients .
- Detailed Description
The aim of this study is to compare the efficacy of ultrasound-guided serratus anterior plane block with bupivacaine/ magnesium versus bupivacaine/ nalbuphine in breast cancer surgery.
Patients and methods nclusion criteria:
-ASA I and II female patients, age 25-60 undergoing breast cancer surgery
Exclusion criteria:
* Patient refusal
* Contraindications for regional blocks (eg. Infection at the injection site, coagulopathy)
* Allergy to the drugs used in the study
* Chronic pain therapy,
* BMI more than 30 kg/m2
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 40
- ASA I and II female patients, age 25-60 undergoing breast cancer surgery
- -Patient refusal
- Contraindications for regional blocks (eg. Infection at the injection site, coagulopathy)
- Allergy to the drugs used in the study
- Chronic pain therapy,
- BMI more than 30 kg/m2
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description GBM:( bupivacaine/magnesium sulphate) serratus anterior plan block serratus plane block will performed in the supine position under strict aseptic conditions before induction of anesthesia. GBM:( bupivacaine/magnesium sulphate): will receive bupivacaine 30 ml 0.25 and 500 mg magnesium sulphate GBN: ( bupivacaine/nalpuphin) serratus anterior plan block serratus plane block will performed in the supine position under strict aseptic conditions before induction of anesthesia.. ( bupivacaine/nalpuphin):received bupivacaine 30 ml 0.25 % and nalpuphine 0.2mg/kg.
- Primary Outcome Measures
Name Time Method time to first analgesic requirements in minutes change from base line for 24 hours time to first analgesic requirements in minutes by the patient
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Faculty Of Medicine, Beni-Suef University
🇪🇬Banī Suwayf, Egypt