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Clinical Trials/CTRI/2021/07/034963
CTRI/2021/07/034963
Not yet recruiting
未知

Comparison of efficacy and safety of nalbuphine, dexmedetomidine and tramadol for treatment of post-spinal shivering in pregnant women undergoing Caesarean section

Government Institute of Medical sciences0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Government Institute of Medical sciences
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
Government Institute of Medical sciences

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients from obstetrics group aged between 20â??40 years of ASA grade I and II undergoing caesarean section.2\. Patients who will give a valid informed written consent.
  • 3\.Patients who will develop shivering of grade 3or4\.

Exclusion Criteria

  • 1\. Patients of age group between 20\-40belonging to ASA grade III and IV.
  • 2\. Patients with known hypersensitivity to tramadol, dexmedetomidine and nalbuphine.
  • 3\. Patients who will not give valid informed consent.
  • 4\. Patients who will have shivering before spinal anaesthesia.
  • 5\. Patients who will have shivering before delivery.
  • 6\. Contraindication of spinal anaesthesia.

Outcomes

Primary Outcomes

Not specified

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