A study to compare the postoperative pain relief for levobupivacaine with fentanyl or dexmedetomidine in below umbilical surgeries in spinal anaesthesia.
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: K400- Bilateral inguinal hernia, with obstruction, without gangreneHealth Condition 2: O- Medical and SurgicalHealth Condition 3: O- Medical and Surgical
- Registration Number
- CTRI/2024/02/062502
- Lead Sponsor
- JLN Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients belonging to ASA (American Society of Anaesthesiologists) class I and II of either sex.
Informed consent.
Exclusion Criteria
Patient’s refusal.
Uncooperative patients.
Any contraindication of spinal block.
Any known hypersensitivity or contraindication to levobupivacaine and fentanyl.
Local pathology at the site of injection or disability limits the performance of the spinal block.
Patient with a history of respiratory, cardiac, endocrinal, hepatic or renal disease (necessitating classification in ASA Class III or above).
Patients having a history of significant neurological, psychiatric, or neuromuscular disorders.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of analgesiaTimepoint: 1 year
- Secondary Outcome Measures
Name Time Method Onset and recovery of sensory block. <br/ ><br>Onset and recovery of motor block. <br/ ><br>The total amount of rescue analgesic in 24 hours <br/ ><br>Hemodynamic changes. <br/ ><br>Adverse effect if any.Timepoint: 1 year