Dorsal Penile nerve block with Bupivacaine for the prevention of catheter related bladder discomfort for patients in ICU.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/04/041748
- Lead Sponsor
- Dr OM SHIVA S T
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients aged between 18 to 65 years
ASA grade I, II and III status patients
Exclusion Criteria
Patients refusal to consent
Patients history of bladder outflow obstruction
Know allergies to any anaesthetic agents
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The incidence and the severity of CRBD, will be assessed according to the following scaling system; No CRBD indicates that there are no complaints of CRBD at all; Mild indicates that complaints of CRBD exists only if the patient was asked about it; Moderate indicates that patient complain of CRBD spontaneously; and Severe indicates that the CRBD causes a spontaneous behavioral response such as flailing limb, strong vocal response, or attempt to pull out catheter.Timepoint: To evaluate the incidence of Catheter Related Bladder Discomfort in a patient getting catheterization, monitored at 15mims, 30mins, 1hour,2hour, 4hour,8hour, 12hour and 24hour respectively.
- Secondary Outcome Measures
Name Time Method To assess the severity of pain by Numerical analogue scoringTimepoint: To evaluate the pain due to Catheter Related Bladder Discomfort in a patient getting catheterization, monitored at 15mims, 30mins, 1hour,2hour, 4hour,8hour, 12hour and 24hour respectively.