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The Effects of Butyrate Enemas on Visceral Perception

Not Applicable
Completed
Conditions
Visceral (Hyper)Sensitivity
Interventions
Registration Number
NCT00726817
Lead Sponsor
Maastricht University Medical Center
Brief Summary

During this double blind, placebo controlled, randomised cross over study, healthy volunteers received an enema once daily for one week containing either placebo (saline), 50mM butyrate or 100mM of butyrate. Before and directly after each test period a barostat protocol was performed to measure parameters for visceral perception.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
11
Inclusion Criteria
  • healthy
Exclusion Criteria
  • age, under 18 or over 65
  • use of pre- or probiotics during study and 3 months previous to study
  • previous bowel complaints
  • gastrointestinal disease or abdominal surgery

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
2Butyrateenemas, once daily, containing 50mM butyrate
1Butyrateenemas, once daily, containing saline
3Butyrateenemas, once daily, containing 100mM butyrate
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Maastricht University

🇳🇱

Maastricht, Limburg, Netherlands

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