Trial | NCT00910832  Report issue

Title

Efficacy of Eductyl® Versus Placebo for Treatment of Dyschesia
Comparative, Randomized, Double-blind Study of the Efficacy of Eductyl® Versus Placebo for Treatment of Patients With Dyschesia Treated by Rectal Rehabilitation

  • Phase

    Phase 4

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    306
The purpose of this study is to assess the efficacy of Eductyl versus placebo for treatment of patients with dyschesia treated by rectal rehabilitation.
Study Started
May 31
2009
Primary Completion
Dec 31
2011
Study Completion
Jun 30
2012
Last Update
Mar 19
2014
Estimate

Drug Eductyl suppository

one suppository every morning during 21 days

Drug Placebo suppository

placebo suppository every morning during 21 days

Eductyl suppository Experimental

Placebo suppository Placebo Comparator

Criteria 

Inclusion Criteria:

Male or female over 18 years
Patients with dyschesia
Prescription of rehabilitation for dyschesia

Exclusion Criteria:

Rectal diseases
Pain killers
Pregnant women
Breast feeding patients
Non-compliant patients
No Results Posted