A study to compare duration of postoperative pain relief for levobupivacaine with or without fentayl in lower abdominal surgeries in spinal anaesthesia.
Not Applicable
Completed
- Conditions
- Health Condition 1: K00-K95- Diseases of the digestive system
- Registration Number
- CTRI/2019/12/022353
- Lead Sponsor
- JLN Medical college hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
Patients belonging to ASA grade 1 & 2
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 limiting the performance of spinal block.
Patient with 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
- Secondary Outcome Measures
Name Time Method