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- Publisher Website: 10.1038/sc.2011.126
- Scopus: eid_2-s2.0-84856683661
- PMID: 22105463
- WOS: WOS:000300125500011
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Article: Efficacy and safety of lithium carbonate treatment of chronic spinal cord injuries: A double-blind, randomized, placebo-controlled clinical trial
Title | Efficacy and safety of lithium carbonate treatment of chronic spinal cord injuries: A double-blind, randomized, placebo-controlled clinical trial | ||||
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Authors | |||||
Keywords | chronic spinal cord injury clinical trial lithium neural regeneration neuropathic pain | ||||
Issue Date | 2012 | ||||
Publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/sc | ||||
Citation | Spinal Cord, 2012, v. 50 n. 2, p. 141-146 How to Cite? | ||||
Abstract | Study design:Lithium has attracted much attention as a neuroregenerative agent for spinal cord injury in animal models. We hypothesized that the lithium can be beneficial to patients with spinal cord injury. The safety and pharmacokinetics of lithium has been studied in our earlier phase I clinical trial, indicating its safety. This is a phase II clinical trial to evaluate its efficacy on chronic spinal cord injury patients. Objectives: The aim of this study was to investigate the efficacy of lithium on chronic spinal cord injury patients. Setting: A major spinal cord injury rehabilitation center in Beijing, China. Methods: Randomized, double-blind, placebo-controlled 6-week parallel treatment arms with lithium carbonate and with placebo. A total of 40 chronic spinal cord injury subjects were recruited. Oral lithium carbonate was titrated or placebo was simulated to maintain the serum lithium level of 0.6-1.2 mmol l -1 for 6 weeks, followed by a 6-month follow-up. The functional outcomes and the neurological classifications, as well as the safety parameters, adverse events and pharmacokinetic data were carefully collected and monitored. Results: No significant changes in the functional outcomes and the neurological classifications were found. The only significant differences were in the pain assessments using visual analog scale comparing the lithium and the placebo group. No severe adverse event was documented in the study. Conclusion: The lithium treatment did not change the neurological outcomes of patients with chronic spinal cord injury. It is worth to investigate whether lithium is effective in the treatment of neuropathic pain in chronic spinal cord injury.Sponsorship:China Spinal Cord Injury Network Company Limited. © 2012 International Spinal Cord Society All rights reserved. | ||||
Persistent Identifier | http://hdl.handle.net/10722/146839 | ||||
ISSN | 2023 Impact Factor: 2.1 2023 SCImago Journal Rankings: 0.826 | ||||
ISI Accession Number ID |
Funding Information: We thank Dr Limin Liao, Dr Lan Sun, Dr Zhigang Chen, Dr Jimin Xu, Ms Mingqin Dong, Dr Xiandi Zhang and Dr Yukun Yang for significant contributions to this phase II clinical study. The study was supported by China Spinal Cord Injury Network Company Limited. | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yang, ML | en_HK |
dc.contributor.author | Li, JJ | en_HK |
dc.contributor.author | So, KF | en_HK |
dc.contributor.author | Chen, JYH | en_HK |
dc.contributor.author | Cheng, WS | en_HK |
dc.contributor.author | Wu, J | en_HK |
dc.contributor.author | Wang, ZM | en_HK |
dc.contributor.author | Gao, F | en_HK |
dc.contributor.author | Young, W | en_HK |
dc.date.accessioned | 2012-05-23T05:42:27Z | - |
dc.date.available | 2012-05-23T05:42:27Z | - |
dc.date.issued | 2012 | en_HK |
dc.identifier.citation | Spinal Cord, 2012, v. 50 n. 2, p. 141-146 | en_HK |
dc.identifier.issn | 1362-4393 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/146839 | - |
dc.description.abstract | Study design:Lithium has attracted much attention as a neuroregenerative agent for spinal cord injury in animal models. We hypothesized that the lithium can be beneficial to patients with spinal cord injury. The safety and pharmacokinetics of lithium has been studied in our earlier phase I clinical trial, indicating its safety. This is a phase II clinical trial to evaluate its efficacy on chronic spinal cord injury patients. Objectives: The aim of this study was to investigate the efficacy of lithium on chronic spinal cord injury patients. Setting: A major spinal cord injury rehabilitation center in Beijing, China. Methods: Randomized, double-blind, placebo-controlled 6-week parallel treatment arms with lithium carbonate and with placebo. A total of 40 chronic spinal cord injury subjects were recruited. Oral lithium carbonate was titrated or placebo was simulated to maintain the serum lithium level of 0.6-1.2 mmol l -1 for 6 weeks, followed by a 6-month follow-up. The functional outcomes and the neurological classifications, as well as the safety parameters, adverse events and pharmacokinetic data were carefully collected and monitored. Results: No significant changes in the functional outcomes and the neurological classifications were found. The only significant differences were in the pain assessments using visual analog scale comparing the lithium and the placebo group. No severe adverse event was documented in the study. Conclusion: The lithium treatment did not change the neurological outcomes of patients with chronic spinal cord injury. It is worth to investigate whether lithium is effective in the treatment of neuropathic pain in chronic spinal cord injury.Sponsorship:China Spinal Cord Injury Network Company Limited. © 2012 International Spinal Cord Society All rights reserved. | en_HK |
dc.language | eng | en_US |
dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/sc | en_HK |
dc.relation.ispartof | Spinal Cord | en_HK |
dc.subject | chronic spinal cord injury | en_HK |
dc.subject | clinical trial | en_HK |
dc.subject | lithium | en_HK |
dc.subject | neural regeneration | en_HK |
dc.subject | neuropathic pain | en_HK |
dc.title | Efficacy and safety of lithium carbonate treatment of chronic spinal cord injuries: A double-blind, randomized, placebo-controlled clinical trial | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | So, KF:hrmaskf@hkucc.hku.hk | en_HK |
dc.identifier.authority | So, KF=rp00329 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1038/sc.2011.126 | en_HK |
dc.identifier.pmid | 22105463 | - |
dc.identifier.scopus | eid_2-s2.0-84856683661 | en_HK |
dc.identifier.hkuros | 199491 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-84856683661&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 50 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 141 | en_HK |
dc.identifier.epage | 146 | en_HK |
dc.identifier.isi | WOS:000300125500011 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Yang, ML=23391357400 | en_HK |
dc.identifier.scopusauthorid | Li, JJ=54958128700 | en_HK |
dc.identifier.scopusauthorid | So, KF=34668391300 | en_HK |
dc.identifier.scopusauthorid | Chen, JYH=54956303400 | en_HK |
dc.identifier.scopusauthorid | Cheng, WS=54958854100 | en_HK |
dc.identifier.scopusauthorid | Wu, J=54958570300 | en_HK |
dc.identifier.scopusauthorid | Wang, ZM=54957062800 | en_HK |
dc.identifier.scopusauthorid | Gao, F=46261070200 | en_HK |
dc.identifier.scopusauthorid | Young, W=8128819100 | en_HK |
dc.identifier.citeulike | 10065230 | - |
dc.identifier.issnl | 1362-4393 | - |