Clinical trial

Study to Assess the Efficacy and Safety of Monthly Octreotide Intramuscular…

NCT00170742 · Novartis, Industry · Terminated

Key facts

NCT number NCT00170742
Title Study to Assess the Efficacy and Safety of Monthly Octreotide Intramuscular Injections in Patients With Proliferative Diabetic Retinopathy After Lasercoagulation This Study is Not Being Conducted in the United States.
Official title A Randomized, Open Label, Controlled Study on the Efficacy and Safety of Octreotide i.m. in Patients With Proliferative Diabetic Retinopathy (PDR) After Start of Laser Coagulation
Lead sponsor Novartis, Industry
Status Terminated
Phase Phase 3
Study type Interventional
Conditions Proliferative Diabetic Retinopathy
Intervention type Drug
Interventions Octreotide, 30 mg i.m. LAR formulation
Enrollment 17
Start date Dec 1, 2003
Primary completion May 1, 2006
First posted Sep 15, 2005
Last update posted Aug 12, 2008
Countries Switzerland

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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