This is a clinical trial to study and compare two drugs, chloroprocaine and bupivacaine for the benefits of patients undergoing short period of surgeries or day procedures who can be discharged early.
Phase 4
Completed
- Conditions
- Health Condition 1: null- Below umbilicus surgeries, lower limb surgeries, anorectal surgeriesHealth Condition 2: O- Medical and SurgicalHealth Condition 3: O- Medical and Surgical
- Registration Number
- CTRI/2018/05/013574
- Lead Sponsor
- Gayatri Vidya parishad institute of health care and medical technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
ASA I-III, Surgical procedures less than 60minutes ( 1 hour) , elective surgeries, below umbilicus procedures (lower limb, ano-rectal, urological, gynecological surgeries)
Exclusion Criteria
patients with contraindications to spinal anaesthesia ( Platelet count < 75,000 , INR >1.5 , use of anti-coagulants, Spinal deformities,, sevre cardiac lesions) , age < 18years > 70years, surgeries lasting more than 60minutes,n patients under ASA IV, V, E, patients allergic or intolerant to local anaesthetic agent, patients who are not willing to be included in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The duration of sensory and motor blockade.Timepoint: 5 minutes to 4 hours
- Secondary Outcome Measures
Name Time Method peak level of blockade, time until ambulation, time to reach eligibility criteria for discharge, complications like transient neurological symptoms (TNS)Timepoint: 5minutes to 12 hours