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Nasogastric Tube Insertion Using Cook Airway Exchange Catheter in Anesthetized Patients

3. februar 2013 opdateret af: Hyeon-Jeong Lee, Pusan National University Hospital
we first examined whether use of tube exchange catheter during NGT insertion could increase the success rate on the first attempt of NGT insertion compared with conventional technique. We then addressed the question of whether the use of tube exchange catheter might decrease the possible occurrence of complication associated with YOON insertion.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Forventet)

100

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiesteder

      • Yangsan, Korea, Republikken
        • Rekruttering
        • Pnuyh Anesthesia
        • Underforsker:
          • JI WOOK YOON, PhD

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

20 år til 70 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • ASA physical status of I or II who were scheduled to undergo elective surgery of gastrointestinal tract with NGT insertion under general anesthesia were enrolled

Exclusion Criteria:

  • Patients with maxillofacial trauma, inability to adequately protect airway, and esophageal abnormalities were excluded. Pregnant patients were also excluded from the study.

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
Ingen indgriben: CONTROL
In the control group (Group A) inserting the lubricated NG tube through the nostril, at that time head maintained in the neutral position.
Aktiv komparator: tube-exchanger
The tube-exchanger group (Group B) made use of tube-exchanger G36402 (CAEC, [cook medical, Bloomington, IN]) as a stylet that was lubricated and inserted within 20-F NGT until the tip of the tube-exchanger was at the tip of the NGT
Andre navne:
  • TUBE EXCHANGER USAGE

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Number of attempt of NGT insertion
Tidsramme: after successful insertion of NGT, within 1 hr

After anesthetic induction, in the control group inserting the lubricated NG tube through the nostril, at that time head maintained in the neutral position. The tube-exchanger group made use of tube-exchanger as stylet within 20-F NGT. Success of appropriate NGT insertion through the nostrils until 70cm of NGT was considered with gurgling sounds on the auscultation over the epigastrium when 10ml of air was injected through the NGT and gastric contents aspiration via NGT. Total number of attempts until successful NGT insertion was recorded and tried at least three times, and was considered to have failed.

Thus, procedure time would be the dependent factor of primary endpoin which could increse the success rate of NGT.

after successful insertion of NGT, within 1 hr
Procedure time of NGT insertion
Tidsramme: after successful insertion of NGT, within 1 hr
After anesthetic induction, in the control group inserting the lubricated NG tube through the nostril, at that time head maintained in the neutral position. The tube-exchanger group made use of tube-exchanger as stylet within 20-F NGT. Success of appropriate NGT insertion was considered with gurgling sounds on the auscultation over the epigastrium when 10ml of air was injected through the NGT and gastric contents aspiration via NGT. NGT insertion time recorded when the NGT begun to insert gently through the nostrils until 70cm of NGT.
after successful insertion of NGT, within 1 hr

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
presence of bleeding of the larynx, and knotting or kinking of NGT under laryngoscopic view
Tidsramme: after successful insertion of NGT within the time of completion of surgery, expected average within 6 hours
The investigators examined the occurrence of complication associated with NGT insertion. After successful NGT insertion, we recorded presence of bleeding of the larynx, and knotting or kinking of NGT using laryngoscopy.
after successful insertion of NGT within the time of completion of surgery, expected average within 6 hours

Samarbejdspartnere og efterforskere

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

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. januar 2013

Primær færdiggørelse (Forventet)

1. februar 2014

Studieafslutning (Forventet)

1. februar 2014

Datoer for studieregistrering

Først indsendt

24. januar 2013

Først indsendt, der opfyldte QC-kriterier

31. januar 2013

Først opslået (Skøn)

4. februar 2013

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

5. februar 2013

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

3. februar 2013

Sidst verificeret

1. februar 2013

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • PNU03-2013-002
  • PNUYH03-2013-002 (Anden identifikator: PUSAN NATIONAL UNIVERSITY YANGSAN HOSPITAL)

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Kliniske forsøg med Elective Surgery of Gastrointestinal Tract

Kliniske forsøg med TUBE EXCHANGER

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