Serratus Plane Block Versus Serratus Plane Block Plus Parasternal Block Combination for Breast Surgery
- Conditions
- AnalgesiaCancer, Breast
- Interventions
- Other: group serratus plan blockOther: group serratus and parasternal plan block
- Registration Number
- NCT05911373
- Lead Sponsor
- Ataturk University
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 64
- American Society of Anesthesiologist's physiologic state I-III patients
- To undergo Mastectomy Surgery
- Being between the ages of 18-65 years
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description group serratus group serratus plan block preoperative superficial serratus block with local anaesthetics and parasternal block with saline group serratus and parasternal group serratus and parasternal plan block preoperative superficial serratus block and parasternal block with local anaesthetics
- Primary Outcome Measures
Name Time Method Postoperative opioid consumption first 24 hours First 24 hours total fentanyl consumption with patient controlled analgesia
- Secondary Outcome Measures
Name Time Method Sensory Assessment 24 hours Sensory Assessment will be performed on patients following the block procedure with pinprick test.
Visual analog pain score First 24 hours Post operative pain will be evaluated with a Visual Analogue Scale (between 0-10; 0: no pain, 10:worst pain) score
Trial Locations
- Locations (1)
Ali Ahiskalioglu
🇹🇷Erzurum, Turkey