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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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16 December 2017 |
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Main ID: |
NCT00879294 |
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Date of registration:
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09/04/2009 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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The Effect of Gum Chewing on Postoperative Ileus
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Scientific title:
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The Effect of Gum Chewing on Postoperative Ileus |
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Date of first enrolment:
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May 2009 |
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Target sample size:
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0 |
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Recruitment status: |
Withdrawn |
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URL:
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https://clinicaltrials.gov/show/NCT00879294 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Single Group Assignment. Primary purpose: Supportive Care. Masking: Single (Investigator).
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Phase:
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N/A
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Countries of recruitment
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United States
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Contacts
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Name:
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Thomas Pranikoff, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Wake Forest University Health Sciences |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- any child who has undergone appendectomy for perforated appendicitis
Exclusion Criteria:
- age less than or equal to 5 years
- unable to chew gum safely
- interval appendectomy
Age minimum:
6 Years
Age maximum:
18 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Perforated Appendicitis
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Intervention(s)
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Dietary Supplement: Chewing Gum
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Device: Motion sickness wristband
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Primary Outcome(s)
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Time to resolution of post-operative ileus.
[Time Frame: 1-14 days]
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Secondary ID(s)
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CR1_IRB00005677
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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