A Comparative study between 0.5% hyperbaric Bupivacaine with 20 mcg Fentanyl when taken in Single syringe and two Separate syringes for Subarachnoid block in Abdominal Hysterectomy
Not Applicable
- Conditions
- Health Condition 1: N859- Noninflammatory disorder of uterus, unspecified
- Registration Number
- CTRI/2021/12/038876
- Lead Sponsor
- Mary Chacko
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASA 1 and 2
2.Age between 30 and 65 year
3.Height between 150 and 180 cm
4.Body Weight between 45 and 75 kgs
5.Patients undergoing Elective Lower Abdominal Hysterectomy
Exclusion Criteria
1.ASA 3 AND 4
2.AGE <30 YEAR AND >65 YEAR
3.BODY WEIGHT <45KG AND >75KG
4.HEIGHT <150CM AND >180CM
5.MENTAL SUBNORMALITY
6.KNOWN ALLERGY TO DRUGS USED IN THE STUDY
7.NEUROLOGICAL OR NEUROMUSCULAR DISORDERS
COAGULATION DISORDER
8.LOCAL INJECTION SITE INFECTIONS
9.PATIENT REFUSA
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset and Duration of Sensory and Motor BlockTimepoint: Starting from the Time of giving Intrathecal injection, Time taken to reach T6 level of block ,Highest level of Block achieved, Time taken for 2 Segment Regression, Time taken to achieve Bromage 3 and Bromage 0 are noted every 2 minutes.Duration of Sensory Block, Total Duration of Analgesia and Duration of Motor Block are calculated from the Above values.
- Secondary Outcome Measures
Name Time Method Hemodynamic parameters- Blood Pressure, Heart RateTimepoint: Monitored Baseline values, every 5 Minutes till 30 Minutes and every 10 Minutes for the next 30 Minutes