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Primary RegistryProtocol numberPublic titleScientific titleType of studyRecruitment statusLast updated
LBCTR2020083421IMR-SCD-301A Phase 2b Study to Evaluate the Safety and Efficacy of IMR-687 in Subjects with Sickle Cell DiseaseA Phase 2b Study to Evaluate the Safety and Efficacy of IMR-687 in Subjects with Sickle Cell DiseaseInterventionalPending26/08/2020
LBCTR2020093402IMR-BTL-201A Phase 2 Study to Evaluate the Safety and Tolerability of IMR-687 in Subjects with Beta ThalassemiaA Phase 2 Study to Evaluate the Safety and Tolerability of IMR-687 in Subjects with Beta ThalassemiaInterventionalPending24/02/2020
LBCTR2019020197ICL670F2202Study to Evaluate Treatment Compliance, Efficacy and Safety of an Improved Deferasirox Formulation (Granules) in Pediatric Patients (2-<18 Years Old) With Iron Overload ( CALYPSO)A randomized, open-label, multicenter, two arm, phase II study to evaluate treatment compliance, efficacy and safety of an improved deferasirox formulation (granules) in pediatric patients with iron overloadInterventionalComplete20/02/2019
LBCTR2020043459HDF 1632The effect of confinement on the mental health of individuals during the COVID-19 pandemic: an online surveyThe effect of confinement on the mental health of individuals during the COVID-19 pandemic: an online survey ObservationalPending16/04/2020
LBCTR2019121361HD2305Preoperative Chlorhexidine Gluconate Bathing Could Prevent Post-obstetric and gynecologic Surgical-site Infections: A Pilot for a Randomized Controlled TrialPreoperative Chlorhexidine Gluconate Bathing Could Prevent Post-obstetric and gynecologic Surgical-site Infections: A Pilot for a Randomized Controlled TrialInterventionalPending24/12/2019
LBCTR2024095653H.pylori-2016-001Comparison of Two Treatment Regimens for Helicobacter pylori Eradication in LebanonA Randomized Prospective and Crossover Study Comparing the Eradication Rate After 10 Days of Concomitant Therapy to Bismuth Quadruple Therapy Among a Sample of the Lebanese PopulationObservationalComplete16/09/2024
LBCTR2021024523GC1801Phase 3 study to evaluate the efficacy and safety of human plasma-derived fibrinogen concentrate (FIB Grifols) in subjects with congenital afibrinogenaemia and severe hypofibrinogenemiaA prospective, multicenter, open-label, single-arm study to evaluate the efficacy and safety of human plasma-derived fibrinogen concentrate (FIB Grifols) in subjects with congenital afibrinogenaemia and severe hypofibrinogenemia requiring either ondemand treatment for acute bleeding or surgical prophylaxisInterventionalPending14/07/2020
LBCTR2020063513GBT440-038Open-Label Extension of VoxelotorAn Open-Label Extension Study of Voxelotor Administered Orally to Participants with Sickle Cell Disease Who Have Participated in Voxelotor Clinical TrialsInterventionalPending12/06/2020
LBCTR2019080216GBT440-034Study to Assess the Effect of Long-term Treatment With GBT440 in Participants Who Have Completed Treatment in Study GBT440-031An Open Label Extension Study of GBT440 Administered Orally to Patients With Sickle Cell Disease Who Have Participated in GBT440 Clinical TrialsInterventionalOther27/03/2019
LBCTR2019080217GBT440-031Study to Evaluate the Effect of Voxelotor Administered Orally to Patients With Sickle Cell Disease (GBT_HOPE)A Phase 3, Double-blind, Randomized, Placebo-controlled, Multicenter Study of Voxelotor Administered Orally to Patients With Sickle Cell DiseaseInterventionalComplete16/07/2020
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