The clomethizole acute stroke study in acute ischemic stroke (class-I): a double blind, parallel group, multinational, multicenter study of the efficacy and safety of i.v. clomethiazole compared to placebo in patients with acute ischemic stroke. Study code: SA-CMZ-0009 (Protocol dated 08/21/97 and Amendment No. 1 dated 06/23/98).,
Role: Investigator,
ASTRA (USA),
(07/2000 - 07/2001)
Status: Completed
Titration to response: Analysis of individualized therapy study (TRAITS) Protocol Capss -048,
Role: Investigator,
Ortho-McNeil Pharmaceutical,
(06/1999 - 06/2000)
Status: Completed
Open-label study to identify the reasons for TASMAR dosage regimen changes in fluctuating Parkinson's disease patients, with follow-up extension,
Role: Investigator,
Hoffmann-La Roche Inc.,
(08/1998 - 08/1999)
Status: Completed
A phase III, multi-center, double-blind, randomized, placebo-controlled, parallel-group study to evaluate the safety and efficacy of a 24-hr infusion of Cervene in patients with acute ischemic stroke,
Role: Investigator,
Baker Norton Pharmaceuticals,
(06/1997 - 06/1998)
Status: Completed
A Trial of Recombinant Methionyl Human Brain-Derived Neurotrophic Factor (r-metHuBDNF) Given by Daily Subcutaneous Injection to Patients with Amyotrophic Lateral Sclerosis (ALS),
Role: Investigator,
Amgen, Inc.,
(07/1996 - 07/1997)
Status: Completed
A Randomized, Triple-Blind, Placebo-Controlled, Outpatient Study to Examine the Safety and Efficacy of 10 mg p.o. MK-462 in the Treatment of Multiple Attacks of Migraine Headache,
Role: Investigator,
Merck, Sharp, and Dohme (MSD) Research Foundation,
(04/1996 - 04/1997)
Status: Completed
A Randomized, Triple Blind, Placebo-Controlled, Outpatient Study to Examine the Safety and Efficacy of 10 mg p.o. MK-0462 in the Treatment of Multiple Attacks of Migraine Headache (Preliminary),
Role: Investigator,
Merck, Sharp, and Dohme (MSD) Research Foundation,
(03/1996 - 03/1997)
Status: Completed
Clinical experience and use of sabril in patients with partial seizures,
Role: Investigator,
Marion Merrell Dow,
(01/1996 - 01/1997)
Status: Completed
A Double-Blind, Placebo-Controlled Study Assessing the Efficacy of Gabapentin in Patients with Amyotrophic Lateral Sclerosis (ALS),
Role: Investigator,
Warner Lambert,
(10/1995 - 10/1996)
Status: Completed
A Trial of Recombinant Methionyl Human Brain-Derived Neurotrophic Factor (r-metHuBDNF)Given by Daily Subcutaneous Injection to Patients with Amyotrophic Lateral Sclerosis (ALS). [Advertising Stage],
Role: Investigator,
Amgen, Inc.,
(07/1995 - 07/1996)
Status: Completed
The BETASERON Patient Experience Study,
Role: Investigator,
National Medical Research Corp.,
(06/1995 - 06/1996)
Status: Completed
Internal
A study of midodrine in patients with neurogenic orthostatic hypotension. Protocol #20.762-999A,
Role: Investigator,
LLU Dept. of Neurology,
(07/1996 - 07/1997)
Status: Completed