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A Study of the Use of Combination of Anti-Cholinergic and Minor Tranquilliser in the Treatment of Non-Cardiac Chest Pain - a Double Blind Placebo Controlled Study
This study is currently recruiting participants.
Study NCT00516854   Information provided by Hospital Authority, Hong Kong
First Received: August 15, 2007   Last Updated: June 23, 2009   History of Changes

August 15, 2007
June 23, 2009
June 2002
 
Symptoms scores, quality of life [ Time Frame: 12 Weeks ]
Same as current
Complete list of historical versions of study NCT00516854 on ClinicalTrials.gov Archive Site
  • Compliance [ Time Frame: 12 Weeks ]
  • Adverse effects [ Time Frame: 12 Weeks ]
Same as current
 
A Study of the Use of Combination of Anti-Cholinergic and Minor Tranquilliser in the Treatment of Non-Cardiac Chest Pain - a Double Blind Placebo Controlled Study
A Study of the Use of Combination of Anti-Cholinergic and Minor Tranquilliser in the Treatment of Non-Cardiac Chest Pain - a Double Blind Placebo Controlled Study

Non-cardiac chest pain is a common clinical problem encountered in our practice but at present, the results of treatments are unsatisfactory. The pathogenesis remains unknown but altered motility of the esophagus and psychological factors including anxiety have been implicated as important factors. Reports of the single use of anticholinergic drugs and anxiolytics have yielded conflicting results, has been demonstrated to yield marginal or of no value. However the use of the combination therapy, especially with a double blind fashion have not been reported. On that basis, we propose to use a combination of anti-cholinergic and tranquilliser for the symptomatic treatment of non-cardiac chest pain. The aim of this study is to evaluate the efficacy of combination therapy of anti-cholinergic and anxiolytic drugs in the treatment of non-cardiac chest pain.

 
 
Interventional
Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Chest Pain
Drug: chlordiazepoxide 5 mg, clidinium 2.5 mg, twice daily
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
100
December 2008
 

Inclusion Criteria:

  • Ambulatory patients over the age of 18
  • Patients who are normal endoscopically
  • Patients who do not have symptomatic reflux disease
  • Patient who have normal coronary angiogram or patient with normal exercise radionuclide scan or patient with normal persantin radionuclide scan.

Exclusion Criteria:

  • Patients with history of significant cardiac, renal, pulmonary or hepatic diseases,
  • Patients with history of dyspepsia or peptic ulcer diseases
  • Patient with documented reflux diseases.
  • Patient on drugs that affect gastrointestinal motility in the past 2 weeks
  • Patients who are pregnant or lactating
  • Patients who are suffering from costochrondritis
  • Patients who are known to be sensitive to benzodiazepine or anti-cholinergic
  • Patients with glaucoma and benign prostatic hypertrophy
Both
18 Years and older
 
Contact: Ting Kin Cheung, Dr (852) 2855 3989 cheungtk@hkucc.hku.hk
China
 
NCT00516854
 
EC1617- 01, HARECCTR0500040
Hospital Authority, Hong Kong
The University of Hong Kong
Principal Investigator: Ting Kin Cheung, Dr Department of Medicine, Queen Mary Hospital/ The University of Hong Kong
Hospital Authority, Hong Kong
June 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP