Evaluation of Pcv-aCO2 in the Fluid Treatment of Abdominal Tumor Patients After Surgery
27. november 2016 opdateret af: Tianjin Medical University Cancer Institute and Hospital
Clinical Study of Central Venous-to-Arterial Carbon Dioxide Difference(Pcv-aCO2) in the Evaluation of Fluid Therapy for Postoperative Patients With Abdominal Cancer
This research will confirm that Pcv-aCO2 is suitable for the guidance of early fluid therapy and the evaluation of the prognosis of patients with abnormal hemodynamics after abdominal tumor surgery, and is expected to be a new monitoring index to improve the therapeutic effect of these patients.
Studieoversigt
Status
Ukendt
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
- Confirmed that Pcv-aCO2 is suitable for the guidance of early fluid therapy and the evaluation of the prognosis of patients with abnormal hemodynamics after abdominal tumor surgery, and is expected to be a new monitoring index to improve the therapeutic efficacy of this kind of patients.
- Pcv-aCO2 effectively reflected the improvement of tissue and organ microcirculation disorder through the individual goal target treatment to guide the fluid resuscitation in the hemodynamic instability patients.
- Research of the correlation between Pcv-aCO2 and the organ function in patients with abnormal hemodynamics after operation.
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
150
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Tianjin
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Tianjin, Tianjin, Kina, 300060
- Rekruttering
- Tianjin Medical University Cancer Institute and Hospital
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Kontakt:
- Wanhua Wang, director
- Telefonnummer: 1021 23340123
- E-mail: Wanhua_Wang1962@outlook.com
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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 til 65 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Acute physiology and chronic health score system II (APACHE II) score ≥10；
- Hemodynamic abnormalities post-operation (a. systolic blood pressure<90mmHg, or descent by basic blood pressure for more than 40mmHg. b. pulse pressure <20mmHg, c. urine volume <0.5ml/Kg/hr, d. heart rate >100 / min, e.Central Venous Pressure(CVP) <5mmHg, f. blood lactic acid >2.7mmol/L, meet any one above).
- Age ≥ 18 years, which is expected to stay in ICU for 5 days or longer;
- Patients themselves or their authorized clients agree to participate in clinical trials and signed informed consent.
Exclusion Criteria:
- age <18 years;
- without improvement in respiratory system disease or chronic obstructive pulmonary disease with Forced expiratory volume in one second (FEV1) <50%;
- lobectomy and pneumonectomy;
- death within 24 after treatment;
- patients with severe organ dysfunction;
- pregnant or lactating women;
- the patients did not sign informed consent;
- any factors that may be expected to increase the risk of patients or other factors that may interfere with the results of clinical trials.
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: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Aktiv komparator: standard group
The patients with ScvO2 ≥ 70% will receive the conventional fluid therapy.than collect the data of ScvO2 and Pcv-aCO2: ScvO2≥70%，and furthermore, Pcv-aCO2 is divided into "≤6mmHg" and ">6mmHg" |
The patients with ScvO2 ≥ 70% will receive the conventional fluid therapy.
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Sham-komparator: control group
The patients with ScvO2 <70% will receive the standardized fluid therapy for 6 hours.than collect the data of ScvO2 and Pcv-aCO2: ScvO2<70%，and furthermore, Pcv-aCO2 is divided into "≤6mmHg" and ">6mmHg" |
The patients with ScvO2 <70% will receive the standardized fluid therapy for 6 hours.
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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The change of Pcv-aCO2
Tidsramme: fluid resuscitation for 6 hours, 12 hours and 24 hours
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The change of Pcv-aCO2 (mmHg) after fluid resuscitation for 6 hours, 12 hours and 24 hours respectively.
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fluid resuscitation for 6 hours, 12 hours and 24 hours
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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The treatment success rate in different groups
Tidsramme: Twenty-eighth days after admission
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Collect the index of treatment success rate(%) of patients in different groups.
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Twenty-eighth days after admission
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The 28 day mortality in different groups
Tidsramme: Twenty-eighth days after admission
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Collect the index of 28 day mortality(%) of patients in different groups.
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Twenty-eighth days after admission
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The hospitalization course in different groups
Tidsramme: Twenty-eighth days after admission
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Collect the index of hospitalization course(days) of patients in different groups.
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Twenty-eighth days after admission
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Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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The change of Central Venous Oxygen Saturation (ScvO2)
Tidsramme: fluid resuscitation for 6 hours, 12 hours and 24 hours
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The change of Central venous oxygen saturation (ScvO2, %)after fluid resuscitation for 6 hours, 12 hours and 24 hours respectively.
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fluid resuscitation for 6 hours, 12 hours and 24 hours
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The change of hemoglobin (Hb)
Tidsramme: fluid resuscitation for 6 hours, 12 hours and 24 hours
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The change of hemoglobin (Hb, g/L) after fluid resuscitation for 6 hours, 12 hours and 24 hours respectively.
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fluid resuscitation for 6 hours, 12 hours and 24 hours
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The change of blood lactic acid (Lac)
Tidsramme: fluid resuscitation for 6 hours, 12 hours and 24 hours
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The change of blood lactic acid (Lac, mmol/L) after fluid resuscitation for 6 hours, 12 hours and 24 hours respectively.
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fluid resuscitation for 6 hours, 12 hours and 24 hours
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The change of Cardiac Index (CI)
Tidsramme: fluid resuscitation for 6 hours, 12 hours and 24 hours
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The change of Cardiac Index (CI, L/(min•m^2)) after fluid resuscitation for 6 hours, 12 hours and 24 hours respectively.
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fluid resuscitation for 6 hours, 12 hours and 24 hours
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The Oxygen Supply status (DO2) in different groups
Tidsramme: fluid resuscitation for 6 hours, 12 hours and 24 hours
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Collect the index of oxygen supply (DO2, ml/(min•m^2)) after fluid resuscitation for 6 hours, 12 hours and 24 hours respectively.
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fluid resuscitation for 6 hours, 12 hours and 24 hours
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The Oxygen Consumption (VO2) in different groups
Tidsramme: fluid resuscitation for 6 hours, 12 hours and 24 hours
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Collect the index of oxygen consumption (VO2, ml/(min•m^2)) after fluid resuscitation for 6 hours, 12 hours and 24 hours respectively.
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fluid resuscitation for 6 hours, 12 hours and 24 hours
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Studieleder: Wanhua Wang, director, Tianjin Medical University Cancer Institute and Hospital
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
- Jones AE, Shapiro NI, Trzeciak S, Arnold RC, Claremont HA, Kline JA; Emergency Medicine Shock Research Network (EMShockNet) Investigators. Lactate clearance vs central venous oxygen saturation as goals of early sepsis therapy: a randomized clinical trial. JAMA. 2010 Feb 24;303(8):739-46. doi: 10.1001/jama.2010.158.
- Futier E, Robin E, Jabaudon M, Guerin R, Petit A, Bazin JE, Constantin JM, Vallet B. Central venous O(2) saturation and venous-to-arterial CO(2) difference as complementary tools for goal-directed therapy during high-risk surgery. Crit Care. 2010;14(5):R193. doi: 10.1186/cc9310. Epub 2010 Oct 29.
- Pope JV, Jones AE, Gaieski DF, Arnold RC, Trzeciak S, Shapiro NI; Emergency Medicine Shock Research Network (EMShockNet) Investigators. Multicenter study of central venous oxygen saturation (ScvO(2)) as a predictor of mortality in patients with sepsis. Ann Emerg Med. 2010 Jan;55(1):40-46.e1. doi: 10.1016/j.annemergmed.2009.08.014. Epub 2009 Oct 25.
- Harilall Y, Adam JK, Biccard BM, Reddi A. Correlation between cerebral tissue and central venous oxygen saturation during off-pump coronary bypass graft surgery. Perfusion. 2011 Mar;26(2):83-90. doi: 10.1177/0267659110387846. Epub 2010 Nov 15.
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. oktober 2016
Primær færdiggørelse (Forventet)
1. januar 2018
Studieafslutning (Forventet)
1. september 2018
Datoer for studieregistrering
Først indsendt
9. oktober 2016
Først indsendt, der opfyldte QC-kriterier
27. november 2016
Først opslået (Skøn)
30. november 2016
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
30. november 2016
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
27. november 2016
Sidst verificeret
1. oktober 2016
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- bc2016032
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
JA
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