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Clinical Trials/IRCT2017030531972N2
IRCT2017030531972N2
Completed
Phase 2

The effect of abdominal massage on gastrointestinal function and aspiration incidence among patients hospitalized in intensive care units in Shahid Bahonar hospital of Kerman University of Medical Sciences in 2017

Vice Chancellor for Research of Kerman University of Medical Sciences0 sites70 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Vice Chancellor for Research of Kerman University of Medical Sciences
Enrollment
70
Status
Completed
Last Updated
8 years ago

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

Sponsor
Vice Chancellor for Research of Kerman University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Over age 18 years up to 70ears; nutrition by nose\-feed tube to enteral feeding alternative methods; have not received metoclopramide, erythromycin, cisapride, and anticholinergic agents; have not received radiotherapy treatment and surgery on the abdominal region in the previous 6 weeks; have no contraindication to abdominal massage for examples: cellulitis, abdominal mass, peritonitis, abdominal aneurysm, ascites (Recognizing doctor), consciousness (GCS) less than 9\.
  • Exclusion criteria: having vomiting (view the contents reflux regardless of its value) (vomiting increase the risk of aspiration effect); NPO for doing laboratory tests and surgical procedures; incidence diarrhea (having 3 or more loose stools per day times the volume More200\-250 cc); discharge from ICU or death less than 3 days; hyperglycemia (blood sugar more than 200\) and hypokalemia (potassium level less than3/5\); GI bleeding (Recognizing doctor); patientes be extubated before 3 day; patients who have aspiration Before entering the study; patientes because of severe trauma have is not been able to get on the suitable position for massage; patientes have spinal cord injury?; incidence ascites during the study.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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