To check the efficacy of 1% chloroprocaine in patients undergoing short surgical procedures below the level of umbilicus
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2020/10/028434
- Lead Sponsor
- Jss hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
ASA CLASS 1 & 2
ELECTIVE SURGERIES
Exclusion Criteria
Patient refusal
Local infection
Allergic to local anaesthetics
Bleeding disorders
Spinal deformity
Cardiac disease
Pregnancy
Hypovolemic shock
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the time required for micturition and ambulationTimepoint: Time for micturition will be assessed after the surgery in the post operative period <br/ ><br>Time for ambulation will be assessed in the post operative period after assessment of all the sensory motor and hemodynamic parameters for mobilization
- Secondary Outcome Measures
Name Time Method To assess the time of onset,time for maximal level of sensory and motor block,duration of sensory and motor block and time taken for regression of sensory and motor blockadeTimepoint: Time of onset: Time taken from the administration of the drug till patient achieves sensory and motor block <br/ ><br>Duration : Time from complete administration of drug till patient regains sensation and able to move lowerlimb <br/ ><br>Time taken for regression is the time when the patient feels the sensation at the s2 segment