{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,17]],"date-time":"2026-06-17T16:05:24Z","timestamp":1781712324102,"version":"3.54.5"},"reference-count":55,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2015,6,13]],"date-time":"2015-06-13T00:00:00Z","timestamp":1434153600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Child Psychology Psychiatry"],"published-print":{"date-parts":[[2016,1]]},"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      Tourette syndrome (\n                      <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content>\n                      ) is a common tic disorder in children and adolescents. There is preliminary evidence that herbal medicine may possess the potential to treat tics. The purpose of this study was to formally evaluate the efficacy and safety of 5\u2010Ling Granule (5\u2010\n                      <jats:styled-content style=\"fixed-case\">LG<\/jats:styled-content>\n                      r), a proprietary polyherbal product, for the treatment of patients with\n                      <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content>\n                      in comparison with tiapride and placebo.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      In this multisite, double\u2010blind, double\u2010dummy, randomized, placebo\u2010controlled trial, 603 patients with\n                      <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content>\n                      aged 5\u201318\u00a0years were randomly assigned to treatment with placebo (\n                      <jats:italic>n<\/jats:italic>\n                      \u00a0=\u00a0117), tiapride (\n                      <jats:italic>n<\/jats:italic>\n                      \u00a0=\u00a0123, 200\u2013400\u00a0mg\/day) or 5\u2010\n                      <jats:styled-content style=\"fixed-case\">LG<\/jats:styled-content>\n                      r (\n                      <jats:italic>n<\/jats:italic>\n                      \u00a0=\u00a0363, 15\u201322.5\u00a0g\/day) for 8\u00a0weeks. The primary outcome was measured using the Yale Global Tic Severity Scale (\n                      <jats:styled-content style=\"fixed-case\">YGTSS<\/jats:styled-content>\n                      ) and its subscales, total tic Score (\n                      <jats:styled-content style=\"fixed-case\">TTS<\/jats:styled-content>\n                      ) and tic\u2010related impairment. Incidence of adverse events was compared among the three groups.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      While tics of all patients were reduced over time, 5\u2010\n                      <jats:styled-content style=\"fixed-case\">LG<\/jats:styled-content>\n                      r and tiapride treatment produced significantly greater improvement on the\n                      <jats:styled-content style=\"fixed-case\">YGTSS<\/jats:styled-content>\n                      overall scale and subscale for\n                      <jats:styled-content style=\"fixed-case\">TTS<\/jats:styled-content>\n                      and impairment at endpoint than the placebo. Seventy\u2010four percentage of patients in the 5\u2010\n                      <jats:styled-content style=\"fixed-case\">LG<\/jats:styled-content>\n                      r arm and 68.3% in the tiapride arm had clinical response and these rates of response were significantly higher than those on placebo (44.0%,\n                      <jats:italic>p\u00a0<\/jats:italic>\n                      &lt;\n                      <jats:italic>\u00a0<\/jats:italic>\n                      .001). The incidence of overall adverse events was significantly fewer for patients on placebo and 5\u2010\n                      <jats:styled-content style=\"fixed-case\">LG<\/jats:styled-content>\n                      r compared to tiapride (11.2% and 13.8% vs. 26.0%,\n                      <jats:italic>p\u00a0<\/jats:italic>\n                      =\n                      <jats:italic>\u00a0<\/jats:italic>\n                      .002); in particular physical tiredness, dizziness and sleep disturbance.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      The clinical efficacy of 5\u2010\n                      <jats:styled-content style=\"fixed-case\">LG<\/jats:styled-content>\n                      r is comparable to tiapride in reducing tics. Its safety profile is better than tiapride. 5\u2010\n                      <jats:styled-content style=\"fixed-case\">LG<\/jats:styled-content>\n                      r can be considered a safe and effective therapy for\n                      <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content>\n                      (Trial registration:\n                      <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"http:\/\/www.clinicaltrials.gov\">www.clinicaltrials.gov<\/jats:ext-link>\n                      :\n                      <jats:styled-content style=\"fixed-case\">NCT<\/jats:styled-content>\n                      01501695).\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jcpp.12432","type":"journal-article","created":{"date-parts":[[2015,6,13]],"date-time":"2015-06-13T02:44:40Z","timestamp":1434163480000},"page":"74-83","source":"Crossref","is-referenced-by-count":64,"title":["A proprietary herbal medicine (5\u2010\n                    <scp>L<\/scp>\n                    ing\n                    <scp>G<\/scp>\n                    ranule) for\n                    <scp>T<\/scp>\n                    ourette syndrome: a randomized controlled trial"],"prefix":"10.1111","volume":"57","author":[{"given":"Yi","family":"Zheng","sequence":"first","affiliation":[{"name":"Beijing Institutes for Brain Disorders Beijing Anding Hospital Capital Medical University Beijing China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhang\u2010Jin","family":"Zhang","sequence":"additional","affiliation":[{"name":"Beijing Institutes for Brain Disorders Beijing Anding Hospital Capital Medical University Beijing China"},{"name":"School of Chinese Medicine LKS Faculty of Medicine The University of Hong Kong Hong Kong China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xin\u2010Min","family":"Han","sequence":"additional","affiliation":[{"name":"Department of Pediatrics The Affiliated Hospital of Nanjing University of Chinese Medicine Nanjing Jiangsu China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ying","family":"Ding","sequence":"additional","affiliation":[{"name":"Department of Pediatrics The First Affiliated Hospital of Henan University of Chinese Medicine Zhengzhou Henan China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yu\u2010Yan","family":"Chen","sequence":"additional","affiliation":[{"name":"Department of Pediatrics The First Affiliated\u00a0Hospital of Zhejiang University of Chinese Medicine Hangzhou Zhejiang China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xue\u2010Feng","family":"Wang","sequence":"additional","affiliation":[{"name":"Department of Pediatrics The Affiliated Hospital of Liaoning University of Chinese Medicine Shenyang Liaoning 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