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Clinical Trials/CTRI/2024/01/061809
CTRI/2024/01/061809
Not yet recruiting
Phase 3

comparison of the effectiveness of injection ropivacaine hydrochloride (0.25%) + injection dexamethasone(1ml) versus injection ropivacaine hydrochloride (0.25%) + injection normal saline(1ml) in ultrasound guided bilateral transverse abdominis plane block for postoperative analgesia in elective abdominal hysterectomy under subarachnoid block: randomized , double blind study.

Goverment Medical College, Bhavnagar0 sites0 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: N959- Unspecified menopausal and perimenopausal disorder
Sponsor
Goverment Medical College, Bhavnagar
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Goverment Medical College, Bhavnagar

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients undergoing elective abdominal
  • hysterectomy under subarachnoid block.
  • 2\. Age: 30\-60 years.
  • 3\. ASA(American society of anaesthesiology)
  • physical status I and II.

Exclusion Criteria

  • 1\. Patients who does not give informed written
  • 2\. History of allergy to study drug (ropivacaine)
  • 3\. patient on any form of analgesic therapy.

Outcomes

Primary Outcomes

Not specified

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