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Clinical Trial Summary

The purpose of this study is to see if GW876008 in Irritable Bowel Syndrome patients will reverse stress-induced hypersensitivity, by looking at thresholds for perception and pain.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00385099
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 2
Start date December 8, 2006
Completion date October 15, 2007

See also
  Status Clinical Trial Phase
Completed NCT01855711 - Safety and Efficacy Study of GR68755 (Alosetron Hydrochloride) to Treat Severe Diarrhea-Predominant Irritable Bowel Syndrome (IBS) Phase 2
Terminated NCT00423345 - Colon Investigation - Factors Determining Choice of Procedure
Completed NCT00101985 - Eight-Weeks Of Treatment With Talnetant In Subjects With Irritable Bowel Syndrome (IBS) Phase 2
Completed NCT00376896 - Study On The Effect Of GW876008 On Cerebral Blood Flow In Irritable Bowel Syndrome (IBS) Patients And Healthy Volunteers Phase 1
Completed NCT00067457 - Study In Women With Severe Diarrhea-Predominant Irritable Bowel Syndrome Having Failed Conventional Therapy Phase 3
Completed NCT00067561 - Study Of Women With Severe Diarrhea-Predominant Irritable Bowel Syndrome Having Failed Conventional Therapy Phase 3
Terminated NCT00461682 - Sb-705498 Rectal Pain Study Phase 2
Completed NCT00370032 - Study to Assess the Effect Of Alosetron On Mucosal Blood Flow Phase 4