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Clinical Trials/CTRI/2017/08/009249
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Department of Anaesthesiology

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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