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Sökning: id:"swepub:oai:DiVA.org:uu-400101" > The proximal hamstr...

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FältnamnIndikatorerMetadata
00006018naa a2200697 4500
001oai:DiVA.org:uu-400101
003SwePub
008191219s2019 | |||||||||||000 ||eng|
009oai:DiVA.org:liu-162772
009oai:prod.swepub.kib.ki.se:142381172
0247 a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4001012 URI
0247 a https://doi.org/10.1136/bmjopen-2019-0316072 DOI
0247 a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-1627722 URI
0247 a http://kipublications.ki.se/Default.aspx?queryparsed=id:1423811722 URI
040 a (SwePub)uud (SwePub)liud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
1001 a Pihl, Elsau Karolinska Institutet4 aut
2451 0a The proximal hamstring avulsion clinical trial (PHACT)-a randomised controlled non-inferiority trial of operative versus non-operative treatment of proximal hamstrings avulsions :b study protocol
264 c 2019-09-13
264 1b BMJ Publishing Group Ltd,c 2019
338 a electronic2 rdacarrier
500 a Funding Agencies|AFA Insurance; Centrum for idrottsforskning, CIF [P2019-0155]; Landstingets Omsesidiga Forsakringsbolag, LOF; Ostergotland County Council
520 a Introduction The treatment of proximal hamstring avulsions is controversial. While several trials have investigated the outcome for patients treated surgically, there is today no prospective trial comparing operative treatment with non-operative treatment. This protocol describes the design for the proximal hamstring avulsion clinical trial (PHACT)-the first randomised controlled trial of operative versus non-operative treatment for proximal hamstring avulsions. Methods and analysis PHACT is a multicentre randomised controlled trial conducted across Sweden, Norway and Finland. Eligible patients (60 participants/treatment arm) with a proximal hamstring avulsion of at least two of three tendons will be randomised to either operative or non-operative treatment. Participants allocated to surgery will undergo reinsertion of the tendons with suture anchors. The rehabilitation programme will be the same for both treatment groups. When patient or surgeon equipoise for treatment alternatives cannot be reached and randomisation therefore is not possible, patients will be invited to participate in a parallel observational non-randomised cohort. The primary outcome will be the patient-reported outcome measure Perth hamstring assessment tool at 24 months. Secondary outcomes include the Lower Extremity Functional Score, physical performance and muscle strength tests, patient satisfaction and MR imaging. Data analysis will be blinded and intention-to-treat analysis will be preformed. Ethics and dissemination Ethical approval has been granted by the Ethical Committee of Uppsala University (DNR: 2017-170) and by the Norwegian ethical board (REC: 2017/1911). The study will be conducted in agreement with the Helsinki declaration. The findings will be disseminated in peer-reviewed publications.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Ortopedi0 (SwePub)302112 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Orthopaedics0 (SwePub)302112 hsv//eng
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Kirurgi0 (SwePub)302122 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Surgery0 (SwePub)302122 hsv//eng
653 a hamstring
653 a hamstring tendons
653 a randomized controlled trial
653 a MRI
653 a patient-reported outcome meassure
653 a muscle strength
7001 a Kristoffersen, Malfrid Holenu Haukeland Hosp, Dept Orthopaed Surg, Bergen, Norway4 aut
7001 a Rosenlund, Anne-Mariu Oslo Univ Hosp, Div Orthopaed Surg, Oslo, Norway4 aut
7001 a Laszlo, Sofiau Uppsala universitet,Ortopedi,Uppsala Univ Hosp, Sweden4 aut0 (Swepub:uu)sofla843
7001 a Berglof, Midau Karolinska Inst, Karolinska Inst Danderyds Sjukhus, Stockholm, Sweden4 aut
7001 a Ribom, Evau Uppsala universitet,Ortopedi,Uppsala Univ Hosp, Sweden4 aut0 (Swepub:uu)evlri676
7001 a Eriksson, Karlu Karolinska Institutet4 aut
7001 a Frihagen, Fredeu Oslo Univ Hosp, Div Orthopaed Surg, Oslo, Norway4 aut
7001 a Mattila, Ville M.u Tampere Univ Hosp, Dept Orthopaed, Tampere, Finland4 aut
7001 a Schilcher, Jörgu Linköpings universitet,Avdelningen för Kirurgi, Ortopedi och Onkologi,Medicinska fakulteten,Region Östergötland, Ortopedkliniken i Linköping4 aut0 (Swepub:liu)jorsc03
7001 a Eklund, Martinu Karolinska Institutet4 aut
7001 a Snellman, Greta,d 1978-u Uppsala universitet,Ortopedi,Uppsala Univ Hosp, Sweden4 aut0 (Swepub:uu)gresn966
7001 a Skorpil, Mikaelu Karolinska Institutet4 aut
7001 a Skoldenberg, Olofu Karolinska Institutet4 aut
7001 a Hedbeck, Carl Johanu Karolinska Inst, Karolinska Inst Danderyds Sjukhus, Stockholm, Sweden4 aut
7001 a Jonsson, Kennethu Uppsala universitet,Ortopedi,Uppsala Univ Hosp, Sweden4 aut0 (Swepub:uu)kennjons
7102 a Karolinska Institutetb Haukeland Hosp, Dept Orthopaed Surg, Bergen, Norway4 org
7730 t BMJ Opend : BMJ Publishing Group Ltdg 9:9q 9:9x 2044-6055
8564 u https://doi.org/10.1136/bmjopen-2019-031607y Fulltext
8564 u https://uu.diva-portal.org/smash/get/diva2:1380896/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
8564 u https://bmjopen.bmj.com/content/bmjopen/9/9/e031607.full.pdf
8564 u https://liu.diva-portal.org/smash/get/diva2:1379754/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-400101
8564 8u https://doi.org/10.1136/bmjopen-2019-031607
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-162772
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:142381172

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