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Clinical Trials/IRCT2013010710841N3
IRCT2013010710841N3CompletedPhase 2

Comparative effect of intravenous acetaminophen and suppository of diclophenac on pain relief after elective cesarean section under spinal anesthesia.

Hamadan University Of Medical Science ,Vice chancellor for research0 sites84 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
84

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 45 years (—)
Sex
Female

Inclusion Criteria

  • Parturients with ASA class 1&2; 18-45 years;candidate for elective cesarean section under spinal anesthesia.
  • Exclusion criteria:Liver disease;Renal disease;Cardiac disease;Hypertension;Peptic ulcer;Pre-eclampsia&EclamsiaDiabetes;Allergic reaction;Emergency cesarean section;Bleeding disorder or Anticuagolant drug History;Increasing ICP;Local skin infection;Neurologic disorders.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Hamadan University Of Medical Science ,Vice chancellor for research

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