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Spots Global Cancer Trial Database for Trial of Chewing Gum to Reduce Post Operative Ileus in Elective Colorectal Surgery

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Trial Identification

Brief Title: Trial of Chewing Gum to Reduce Post Operative Ileus in Elective Colorectal Surgery

Official Title: Randomised Controlled Trial of Chewing Gum to Reduce Post Operative Ileus in Elective Colorectal Surgery

Study ID: NCT02372500

Interventions

Chewing gum

Study Description

Brief Summary: It is unknown whether post operative chewing gum will reduce post operative ileus. This study is a randomised controlled trial that will determine whether chewing gum three times a day following surgery will reduce post operative ileus. Time to passage of flatus will be used to determine that incidence of ileus.

Detailed Description: Patients will be randomised to one of two arms, the experimental arm will be chewing gum and the control arm will be normal post operative care. The primary endpoint is time to passage of flatus (defined as end of operation to first passage of flatus, in minutes). The trial will be unblinded to patients and observers and has been powered to demonstrate a 15% reduction in passage to flatus (130 patients required)

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Countess of Chester Hospital, Chester, Cheshire, United Kingdom

Contact Details

Name: Dale Vimalachandran, MD FRCS

Affiliation: Countess of Chester

Role: STUDY_DIRECTOR

Name: Rachel Clifford, MRCS

Affiliation: Countess of Chester

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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