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Clinical Trials/IRCT20191104045328N24
IRCT20191104045328N24
Not yet recruiting
Phase 3

Comparison of the effect of remifentanil and apotel on pain control of laparotomy using a pain pump

Arak University of Medical Sciences0 sites70 target enrollmentTBD
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ConditionsPostoperative Pain.Acute pain, not elsewhere classifiedG89.1

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Postoperative Pain.
Sponsor
Arak University of Medical Sciences
Enrollment
70
Status
Not yet recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Candidates for emergency laparotomy include cancer of abdominal organs, peritonitis, appendicitis, pancreatitis, abscess, adhesions (after trauma or surgery), diverticulitis, intestinal perforation or obstruction, foreign bodies and internal bleeding in accessible spaces.
  • •Aged 18 to 65 years
  • •Consent of the participants to participate in the study

Exclusion Criteria

  • •Addiction to any drug
  • •Known hypersensitivity to remifentanil or Apotel
  • •Complicated laparotomy
  • •Laparotomy with long unconventional time
  • •Wound infection

Outcomes

Primary Outcomes

Not specified

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