CTRI/2017/08/009249
Not yet recruiting
Phase 4
â??Clinical evaluation of efficacy and safety of transversus abdominis plane block inj. Bupivacaine vs. inj. Ropivacaine for post operative analgesia following lower segment cesarean section: a prospective, randomized, controlled, double blind study.â??
Department of Anaesthesiology0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Department of Anaesthesiology
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •ï??Informed written consent for
- •participation in study.
- •ï??Age: 20\-35 years
- •ï??Gender: Antenatal female patients
- •scheduled for elective or non urgent
- •lower segment cesarean section.
- •ï??ASA physical status I and II.
- •ï??Patients refusing consent.
Exclusion Criteria
- •1\.Contraindications to Spinal Anaesthesia like,
- •Local infection or sepsis at the site of
- •Lumbar puncture
- •Bleeding disorders, thrombocytopenia
- •Space occupying lesions of the brain
- •Anatomical disorders of the spine
- •Hypovolaemia e.g. following massive
- •haemorrhage
- •2\.Allergy to local anaesthetic drugs and NSAIDS.
- •3\.Patient on any form of analgesics therapy.
Outcomes
Primary Outcomes
Not specified
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