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Skeletal Muscle Strain Injuries and the Connective Tissue: Characterization, Recovery and Optimal Treatment

25. juli 2017 opdateret af: Monika Lucia Bayer, Bispebjerg Hospital

Firstly, the investigators aim to study the biochemical, structural and functional changes associated with acute muscle strain injury in the acute phase and during rehabilitation in vivo. Specific factors present after the injury and their effects on connective tissue cells will be examined in vitro.

Secondly, the investigators will investigate individuals with chronic pain, scar tissue and inferior function after a previous muscle strain injury and test a specific rehabilitation program to alleviate pain and disabilities associated with the preceding muscle injury. The investigators have the following hypotheses:

  1. Humoral growth factors and pro-inflammatory macrophages released into the injured area post strain injury stimulate formation of connective tissue in vitro.
  2. Early onset of rehabilitation will be superior to a delayed start of rehabilitation for the healing process, in regards to structural improvement of tissue and better clinical function.
  3. Scar tissue following a muscle strain injury is characterized by disorganized structure of connective tissue.
  4. Mechanical loading in the form of heavy eccentric muscle activity for 12 weeks will lead to a local re-modeling of scar tissue, and result in improved function and reduced symptoms in patients with chronic pain and impaired function after a previous muscle injury.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

85

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Danmark
      • Copenhagen, Danmark, 2400
        • Institute of Sports Medicine Copenhagen, Bispebjerg Hospital, Bispebjerg Bakke 23, Building 8

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Acute muscle strain injury
  • Chronic muscle strain injury
  • Age above 18 years

Exclusion Criteria:

  • Daily intake of non-steroidal anti-inflammatory drugs (NSAIDs) within three months prior to the injury
  • Smoking
  • Diabetes
  • Connective tissue and/or rheumatic diseases
  • Any observed organ dysfunctions

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Chronic Exercise
Procedure: Chronic Exercise
Exercise
Eksperimentel: Acute Early onset of rehabilitation
Procedure: Acute Early onset of rehabilitation
Early onset of rehabilitation
Eksperimentel: Chronic control
Procedure: Chronic Control
Control
Eksperimentel: Acute Delayed onset of rehabilitation
Procedure: Acute Delayed onset of rehabilitation
Delayed onset of rehabilitation

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Return to full physical activity
Tidsramme: Baseline; Up to 30 weeks (estimated time frame maximum)
First time the subject is fully fit to take part in all types of physical activity post injury;
Baseline; Up to 30 weeks (estimated time frame maximum)

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Magnetic resonance images
Tidsramme: Baseline, 4 weeks, 6 weeks, 12 weeks, 6 months
Size of injured tissue; Size and location of hematoma; Measurement of muscle perfusion (indication of metabolic activity)
Baseline, 4 weeks, 6 weeks, 12 weeks, 6 months
Ultrasound images
Tidsramme: Baseline, 7-14 days, 4 weeks, 6 weeks, 12 weeks, 6 months
Size and location of injury
Baseline, 7-14 days, 4 weeks, 6 weeks, 12 weeks, 6 months
Ultrasound images
Tidsramme: Baseline, 1 week, 2 weeks
Volume of hematoma
Baseline, 1 week, 2 weeks
Strength measurements
Tidsramme: Baseline, 4 weeks, 6 weeks, 9 weeks, 12 weeks, 6 months
Strength tests of injured muscle group compared to healthy muscle group on contralateral leg
Baseline, 4 weeks, 6 weeks, 9 weeks, 12 weeks, 6 months
Structural changes of tissue
Tidsramme: Baseline, 12 weeks
Evaluation of tissue samples from injured muscle before and after rehabilitation program
Baseline, 12 weeks
Aspiration and characterization of inter-/ intramuscular fluid in the injured muscle
Tidsramme: Baseline, 3 -14 days
The aspirated fluid (hematoma/exudate) will be analyzed for released humoral factors, cell types present and its effect on human fibroblast proliferation
Baseline, 3 -14 days

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Pain score on the Visual Analog Scale
Tidsramme: Baseline, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 weeks
Each subject is asked to rate his/ her pain level on the Visual Analog Scale during each rehabilitation session at a pre-defined time points during the work-out.
Baseline, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 weeks
Injury screening questionnaire
Tidsramme: Baseline, 1,2,3,4,5,6,7,8,9,10,11,12 weeks, 6 and 12 months
Each subject is asked to fill out a questionnaire to record the impact of the injury on his/her physical activity and activities of daily living.
Baseline, 1,2,3,4,5,6,7,8,9,10,11,12 weeks, 6 and 12 months
Rehabilitation registration
Tidsramme: Baseline, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 weeks
Each subject is asked to keep a regular training diary of his/ her rehabilitation progress.
Baseline, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 weeks

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Bispebjerg Hospital

Samarbejdspartnere

University of Copenhagen

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. april 2014

Primær færdiggørelse (Faktiske)

1. december 2016

Studieafslutning (Faktiske)

1. marts 2017

Datoer for studieregistrering

Først indsendt

23. maj 2014

Først indsendt, der opfyldte QC-kriterier

30. maj 2014

Først opslået (Skøn)

2. juni 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

26. juli 2017

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

25. juli 2017

Sidst verificeret

1. juli 2017

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • MI-114

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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