Efficacy of Triprolidine in the Treatment of Temporary Sleep Disturbance
Triprolidine, a first‐generation antihistamine for allergic rhinitis, has a shorter half‐life and fewer persistent effects relative to other antihistamines and may be useful in the treatment of temporary sleep disturbance. Patients aged ≥18 years old were randomized 1:1:1 to receive either triprolid...
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Veröffentlicht in: | Journal of clinical pharmacology 2021-09, Vol.61 (9), p.1156-1164 |
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description | Triprolidine, a first‐generation antihistamine for allergic rhinitis, has a shorter half‐life and fewer persistent effects relative to other antihistamines and may be useful in the treatment of temporary sleep disturbance. Patients aged ≥18 years old were randomized 1:1:1 to receive either triprolidine 2.5 mg (n = 65), triprolidine 5 mg (n = 66), or placebo (n = 67) on 3 consecutive nights. Sleep disturbance index was monitored via wrist actimeter. Subjective measures were assessed via diary card. Triprolidine 2.5 mg had a significantly lower sleep disturbance index versus placebo on night 1 (P = .02); however, when adjusted for outliers, sleep disturbance index did not significantly differ between either dose of triprolidine versus placebo on night 1. Adjusted sleep disturbance index was significantly lower with triprolidine 2.5 and 5 mg versus placebo on night 3 (P = .0017 and P = .011, respectively) and for the mean of all 3 nights (P = .01 and P = .015, respectively). Sleep latency was significantly improved for triprolidine 2.5 mg versus placebo on nights 2 and 3 and for the mean of all 3 nights and for triprolidine 5 mg versus placebo for the mean of all 3 nights. Subjective measures showed those on both doses of triprolidine felt more refreshed on awakening versus placebo for the mean of all 3 nights, with no increase in daytime sleepiness. The frequency of adverse events was similar across groups. The optimum dose of triprolidine for treatment of temporary sleep disturbance was 2.5 mg. There were improvements in both objective and subjective measures of sleep quality versus placebo, with no safety concerns raised. |
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Patients aged ≥18 years old were randomized 1:1:1 to receive either triprolidine 2.5 mg (n = 65), triprolidine 5 mg (n = 66), or placebo (n = 67) on 3 consecutive nights. Sleep disturbance index was monitored via wrist actimeter. Subjective measures were assessed via diary card. Triprolidine 2.5 mg had a significantly lower sleep disturbance index versus placebo on night 1 (P = .02); however, when adjusted for outliers, sleep disturbance index did not significantly differ between either dose of triprolidine versus placebo on night 1. Adjusted sleep disturbance index was significantly lower with triprolidine 2.5 and 5 mg versus placebo on night 3 (P = .0017 and P = .011, respectively) and for the mean of all 3 nights (P = .01 and P = .015, respectively). Sleep latency was significantly improved for triprolidine 2.5 mg versus placebo on nights 2 and 3 and for the mean of all 3 nights and for triprolidine 5 mg versus placebo for the mean of all 3 nights. Subjective measures showed those on both doses of triprolidine felt more refreshed on awakening versus placebo for the mean of all 3 nights, with no increase in daytime sleepiness. The frequency of adverse events was similar across groups. The optimum dose of triprolidine for treatment of temporary sleep disturbance was 2.5 mg. There were improvements in both objective and subjective measures of sleep quality versus placebo, with no safety concerns raised.</description><identifier>ISSN: 0091-2700</identifier><identifier>EISSN: 1552-4604</identifier><identifier>DOI: 10.1002/jcph.1861</identifier><identifier>PMID: 33768603</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adult ; Adverse events ; Allergic rhinitis ; Antihistamines ; Dose-Response Relationship, Drug ; Double-Blind Method ; Female ; Histamine H1 Antagonists - administration & dosage ; Histamine H1 Antagonists - adverse effects ; Histamine H1 Antagonists - therapeutic use ; Humans ; insomnia ; Latency ; Male ; Middle Aged ; over‐the‐counter drugs ; Placebos ; Sleep ; Sleep and wakefulness ; Sleep Latency - drug effects ; Sleep Quality ; Sleep Wake Disorders - drug therapy ; temporary sleep disturbance ; Triprolidine ; Triprolidine - administration & dosage ; Triprolidine - adverse effects ; Triprolidine - therapeutic use ; Wrist</subject><ispartof>Journal of clinical pharmacology, 2021-09, Vol.61 (9), p.1156-1164</ispartof><rights>2021, The American College of Clinical Pharmacology</rights><rights>2021, The American College of Clinical Pharmacology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3131-1ff13632e4b2ca8f82bd01f453721126d366b31a469889bcf44977564869523d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcph.1861$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcph.1861$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33768603$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cravo, Ana Santos</creatorcontrib><creatorcontrib>Shephard, Adrian</creatorcontrib><creatorcontrib>Shea, Tim</creatorcontrib><title>Efficacy of Triprolidine in the Treatment of Temporary Sleep Disturbance</title><title>Journal of clinical pharmacology</title><addtitle>J Clin Pharmacol</addtitle><description>Triprolidine, a first‐generation antihistamine for allergic rhinitis, has a shorter half‐life and fewer persistent effects relative to other antihistamines and may be useful in the treatment of temporary sleep disturbance. Patients aged ≥18 years old were randomized 1:1:1 to receive either triprolidine 2.5 mg (n = 65), triprolidine 5 mg (n = 66), or placebo (n = 67) on 3 consecutive nights. Sleep disturbance index was monitored via wrist actimeter. Subjective measures were assessed via diary card. Triprolidine 2.5 mg had a significantly lower sleep disturbance index versus placebo on night 1 (P = .02); however, when adjusted for outliers, sleep disturbance index did not significantly differ between either dose of triprolidine versus placebo on night 1. Adjusted sleep disturbance index was significantly lower with triprolidine 2.5 and 5 mg versus placebo on night 3 (P = .0017 and P = .011, respectively) and for the mean of all 3 nights (P = .01 and P = .015, respectively). Sleep latency was significantly improved for triprolidine 2.5 mg versus placebo on nights 2 and 3 and for the mean of all 3 nights and for triprolidine 5 mg versus placebo for the mean of all 3 nights. Subjective measures showed those on both doses of triprolidine felt more refreshed on awakening versus placebo for the mean of all 3 nights, with no increase in daytime sleepiness. The frequency of adverse events was similar across groups. The optimum dose of triprolidine for treatment of temporary sleep disturbance was 2.5 mg. There were improvements in both objective and subjective measures of sleep quality versus placebo, with no safety concerns raised.</description><subject>Adult</subject><subject>Adverse events</subject><subject>Allergic rhinitis</subject><subject>Antihistamines</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Histamine H1 Antagonists - administration & dosage</subject><subject>Histamine H1 Antagonists - adverse effects</subject><subject>Histamine H1 Antagonists - therapeutic use</subject><subject>Humans</subject><subject>insomnia</subject><subject>Latency</subject><subject>Male</subject><subject>Middle Aged</subject><subject>over‐the‐counter drugs</subject><subject>Placebos</subject><subject>Sleep</subject><subject>Sleep and wakefulness</subject><subject>Sleep Latency - drug effects</subject><subject>Sleep Quality</subject><subject>Sleep Wake Disorders - drug therapy</subject><subject>temporary sleep disturbance</subject><subject>Triprolidine</subject><subject>Triprolidine - administration & dosage</subject><subject>Triprolidine - adverse effects</subject><subject>Triprolidine - therapeutic use</subject><subject>Wrist</subject><issn>0091-2700</issn><issn>1552-4604</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10MtKxDAUBuAgijNeFr6AFNzoojM5SZqmSxkvowgKjuvQpgmToTeTFpm3N3PRheDqwOHj55wfoQvAE8CYTFeqW05AcDhAY0gSEjOO2SEaY5xBTFKMR-jE-xXGwFkCx2hEacoFx3SM5vfGWJWrddSaaOFs59rKlrbRkW2ifqnDTud9rZt-C3TdtS536-i90rqL7qzvB1fkjdJn6Mjkldfn-3mKPh7uF7N5_PL6-DS7fYkVBQoxGAOUU6JZQVQujCBFicGwhKYEgPCScl5QyBnPhMgKZRjL0jThTPAsIbSkp-h6lxsu_Ry072VtvdJVlTe6HbwkCeYk5aGWQK_-0FU7uCZcF1QQqWAggrrZKeVa7502snO2Dj9KwHJTr9zUKzf1Bnu5TxyKWpe_8qfPAKY78GUrvf4_ST7P3ubbyG9kI4Gn</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Cravo, Ana Santos</creator><creator>Shephard, Adrian</creator><creator>Shea, Tim</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>202109</creationdate><title>Efficacy of Triprolidine in the Treatment of Temporary Sleep Disturbance</title><author>Cravo, Ana Santos ; Shephard, Adrian ; Shea, Tim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3131-1ff13632e4b2ca8f82bd01f453721126d366b31a469889bcf44977564869523d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Adverse events</topic><topic>Allergic rhinitis</topic><topic>Antihistamines</topic><topic>Dose-Response Relationship, Drug</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Histamine H1 Antagonists - administration & dosage</topic><topic>Histamine H1 Antagonists - adverse effects</topic><topic>Histamine H1 Antagonists - therapeutic use</topic><topic>Humans</topic><topic>insomnia</topic><topic>Latency</topic><topic>Male</topic><topic>Middle Aged</topic><topic>over‐the‐counter drugs</topic><topic>Placebos</topic><topic>Sleep</topic><topic>Sleep and wakefulness</topic><topic>Sleep Latency - drug effects</topic><topic>Sleep Quality</topic><topic>Sleep Wake Disorders - drug therapy</topic><topic>temporary sleep disturbance</topic><topic>Triprolidine</topic><topic>Triprolidine - administration & dosage</topic><topic>Triprolidine - adverse effects</topic><topic>Triprolidine - therapeutic use</topic><topic>Wrist</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cravo, Ana Santos</creatorcontrib><creatorcontrib>Shephard, Adrian</creatorcontrib><creatorcontrib>Shea, Tim</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cravo, Ana Santos</au><au>Shephard, Adrian</au><au>Shea, Tim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of Triprolidine in the Treatment of Temporary Sleep Disturbance</atitle><jtitle>Journal of clinical pharmacology</jtitle><addtitle>J Clin Pharmacol</addtitle><date>2021-09</date><risdate>2021</risdate><volume>61</volume><issue>9</issue><spage>1156</spage><epage>1164</epage><pages>1156-1164</pages><issn>0091-2700</issn><eissn>1552-4604</eissn><abstract>Triprolidine, a first‐generation antihistamine for allergic rhinitis, has a shorter half‐life and fewer persistent effects relative to other antihistamines and may be useful in the treatment of temporary sleep disturbance. Patients aged ≥18 years old were randomized 1:1:1 to receive either triprolidine 2.5 mg (n = 65), triprolidine 5 mg (n = 66), or placebo (n = 67) on 3 consecutive nights. Sleep disturbance index was monitored via wrist actimeter. Subjective measures were assessed via diary card. Triprolidine 2.5 mg had a significantly lower sleep disturbance index versus placebo on night 1 (P = .02); however, when adjusted for outliers, sleep disturbance index did not significantly differ between either dose of triprolidine versus placebo on night 1. Adjusted sleep disturbance index was significantly lower with triprolidine 2.5 and 5 mg versus placebo on night 3 (P = .0017 and P = .011, respectively) and for the mean of all 3 nights (P = .01 and P = .015, respectively). Sleep latency was significantly improved for triprolidine 2.5 mg versus placebo on nights 2 and 3 and for the mean of all 3 nights and for triprolidine 5 mg versus placebo for the mean of all 3 nights. Subjective measures showed those on both doses of triprolidine felt more refreshed on awakening versus placebo for the mean of all 3 nights, with no increase in daytime sleepiness. The frequency of adverse events was similar across groups. The optimum dose of triprolidine for treatment of temporary sleep disturbance was 2.5 mg. There were improvements in both objective and subjective measures of sleep quality versus placebo, with no safety concerns raised.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33768603</pmid><doi>10.1002/jcph.1861</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Adverse events Allergic rhinitis Antihistamines Dose-Response Relationship, Drug Double-Blind Method Female Histamine H1 Antagonists - administration & dosage Histamine H1 Antagonists - adverse effects Histamine H1 Antagonists - therapeutic use Humans insomnia Latency Male Middle Aged over‐the‐counter drugs Placebos Sleep Sleep and wakefulness Sleep Latency - drug effects Sleep Quality Sleep Wake Disorders - drug therapy temporary sleep disturbance Triprolidine Triprolidine - administration & dosage Triprolidine - adverse effects Triprolidine - therapeutic use Wrist |
title | Efficacy of Triprolidine in the Treatment of Temporary Sleep Disturbance |
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