WHO ICTRP trial

A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled…

PER-071-01 · Registro Peruano de Ensayos Clínicos (REPEC) · Not Recruiting

Key facts

Trial ID PER-071-01
Public title A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerabllity of 24 Weeks of Nateglinide, Giibenciamide, or Placebo Treatment in Eiderly Type 2 Diabetes Mellitus Patients
Scientific title A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerabllity of 24 Weeks of Nateglinide, Giibenciamide, or Placebo Treatment in Eiderly Type 2 Diabetes Mellitus Patients
Primary sponsor NOVARTIS BIOSCIENSES PERU S.A.,
Registry Registro Peruano de Ensayos Clínicos (REPEC)
Recruitment status Not Recruiting
Study type Interventional
Phase III
Conditions -E119 Non-insulin-dependent diabetes mellitus, without complications Non-insulin-dependent diabetes mellitus, without complications;E119;Non-insulin-dependent diabetes mellitus, without complications
Interventions Group name:Group 1 Type of group;1 N° of participants:220 Intervention(s) description:Nateglinide active from 60 mg ac to 180 mg ac + Glibenclamide placebo; for 24 weeks Group name:Group 3 Type of group;2 N° of participants:110…
Registration date Nov 22, 2001
Target size 0
Registry page ins.gob.pe

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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