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Clinical Trials/IRCT201112078322N1
IRCT201112078322N1
Completed
Phase 4

Evaluating the effect of intravenous Paracetamol or Diclofenac Sodium suppositories on the need for intravenous narcotic administration for pain relief in patients underwent gastrectomy

Mashhad University of Medical Sciences0 sites88 target enrollmentTBD
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ConditionsGastric surgery.Acquired absence of part of stomach

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Gastric surgery.
Sponsor
Mashhad University of Medical Sciences
Enrollment
88
Status
Completed
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\. Patients with gastric cancer who are candidate for gastrectomy
  • •2\. Age range between 40 to70 years
  • •3\. Ability to understand PCA pump use
  • •Exclusion criteria:
  • •1\. History of allergy to morphine, acetaminophen, and diclofenac sodium
  • •2\. History of heart failure (EF\<40%), kidney failure (C2\>2\), moderate to severe COPD
  • •3\. Weight over 10 kilograms or less than 50 kilograms
  • •4\. Long\-term use of opioids before surgery (for more than 2 weeks continuously)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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