drugset / Trial / NCT01624571

Study to Assess the Effect on Recovery of GI Motility and Safety and to Determine the Optimal Dose of LD02GIFRO

NCT01624571 ↗

Phase 2 Completed 147 enrolled LG Life Sciences
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This clinical trial is conducted to determine the optimal dose of LD02GIFRO in improvement of gastrointestinal motility between each dose group by comparing the effectiveness and safety in patients undergoing colon resection.

Timeline

Start
2012-03
Primary completion
2012-10
Completion
2012-10

Drugs

EvaluationDrugModalityDoseRoute
Subject LD02GIFRO Unknown 300 mg —
Subject LD02GIFRO Unknown 600 mg —
Subject LD02GIFRO Unknown 900 mg —

Indications

No indication recorded.