Thoracic paravertebral block noble approach for opiod free analgesia and anaesthesia in breast cancer surgeries.
Not Applicable
- Conditions
- Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
- Registration Number
- CTRI/2020/05/025035
- Lead Sponsor
- nil
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade 1 and 2 female patients. Age group of 18 to 60 years.Patients giving valid informed consent.
Exclusion Criteria
Patient refusal Patients belonging to ASA grade 3 and grade 4
Patients with copd or any pulmonary pathology
Patients with difficult airways Patients with history of drug allergy
Patients with localized skin infections, hemorrhagic diathesis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)To analyze and compare intra operative anesthetic and analgesic properties of usg guided thoracic paravertebral block with control group <br/ ><br>2)To access postoperative analgesic efficacy of usg guided thoracic paravertebral block using vas score and rescue analgesia as compared to control group <br/ ><br>Timepoint: 24 hrs <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1)To compare intraoperative consumption of anesthetic agents in test group and control group <br/ ><br>2)To compare intraoperative and postoperative consumption of analgesic agents <br/ ><br>Timepoint: 24 hrs