Efficacy of Valproate in Peripheral Neuropathic Pain
Efficacy of a Therapeutic Strategy in Peripheral Neuropathic Pain: Intravenous Sodium Valproate Followed by Oral Route Treatment Versus Placebo (Clinical and Neurophysiologic Evaluation)
Sponsor: Sanofi-Synthelabo
Terminated
slow recruitment and treatments beyond expiry date
Other terminated trials from Sanofi-Synthelabo
More terminations from Sanofi-Synthelabo
Other Neuralgia trials with similar outcome
This PHASE2/PHASE3 trial investigates Neuralgia and Neuropathic Peripheral Pain and is currently terminated or withdrawn. Sanofi-Synthelabo leads this study, which shows 5 recorded versions since 2002 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
5 versions recorded-
Sep 2024 — Present [monthly]
Terminated PHASE2/PHASE3
-
Jul 2024 — Sep 2024 [monthly]
Terminated PHASE2/PHASE3
Phase: PHASE2_PHASE3 → PHASE2/PHASE3
-
Jan 2021 — Jul 2024 [monthly]
Terminated PHASE2_PHASE3
-
Jun 2018 — Jan 2021 [monthly]
Terminated PHASE2_PHASE3
-
Jan 2017 — Jun 2018 [monthly]
Terminated PHASE2_PHASE3
First recorded
Mar 2002
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Sanofi-Synthelabo
- University Hospital, Bordeaux
For direct contact, visit the study record on ClinicalTrials.gov .