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Estimation of Pain During Epidural Analgesia During Labor (PERIDANS)

15. september 2015 opdateret af: Centre Hospitalier Universitaire de Saint Etienne

Estimation of Pain During Epidural Analgesia During Labor - a Monocentric Study

Epidural regional anesthesia is a technique to eliminate or lessen pain during obstetric labor and childbirth. It consists in establishing a catheter into the epidural space and to block the transmission of pain sensations by injecting a local anesthetic and an opioid. In 10-25% of cases the epidural does not give perfect results, causing it to test its effectiveness, which is mainly done by questioning the patient on mitigation or disappearance of pain. This collaboration of patients is sometimes limited in our care structure by the inability to assess or express the pain, mainly due to cultural differences or language barriers, which can represent up to 15% of women in our institution. This led to develop objective measures of pain techniques used at the bedside.

Pupil diameter (PD) varies under the double influence of sympathetic system (Σ), dilator of the pupil, and parasympathetic system (pΣ).

The PD increases in response to painful stimulation, in proportion to the intensity of the nociceptive stimulus. This variation of PD has been proposed as a means of evaluation of pain in patients under general anesthesia, but has been little studied in conscious subjects.

There are other permanent changes in the PD, due to constant interaction between Σ and pΣ systems. Few data have been published to date on this PD variability (PDV).

Studieoversigt

Status

Afsluttet

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

40

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiesteder

      • Saint-Etienne, Frankrig, 42055
        • CHU Saint-étienne

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 45 år (Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Kvinde

Beskrivelse

Inclusion Criteria:

  • Obstetrical Labor
  • Able to rate their pain using VAS
  • dilatation of the cervix under 6 centimeters
  • Written consent

Exclusion Criteria:

  • - Not having a anesthesia consultation during the 48 hours before delivery
  • With a contra-indication for an epidural
  • To which an incident occurred during a previous epidural using a medication used in the study
  • Operated a unilateral or bilateral ocular surgery modifying the possibilities of variation of pupil diameter
  • general anesthesia in the seven days preceding delivery
  • Carry a pacemaker or heart grafted
  • Having Parkinson's disease history, insulin or non-insulin diabetes or chronic alcoholism
  • Having cardiac arrhythmia (atrial fibrillation or frequent extrasystoles)
  • Treated for hypertension by receptor antagonists of angiotensin type 2
  • anti-arrhythmic treatment or blocker,
  • Refusing to participate in the study
  • With a contra-indication for the use of ropivacaine and sufentanil.

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Patients

Pain assess by :

  • Visual Analogic Scale (VAS).
  • Portable video pupillometer
Portable video pupillometer measures pupil diameter (PD) in patient during obstetrical labor

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Pupil diameter variability
Tidsramme: From baseline to fifteen minutes after start of Epidural regional anesthesia
Compare Pupil Diameter Variability (PDV) measured before Epidural regional anesthesia and after Epidural regional anesthesia. PDV is aera under the curve of Pupil Diameter from start of the contraction (baseline) to time to peak of the contraction.
From baseline to fifteen minutes after start of Epidural regional anesthesia

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
pupil diameter
Tidsramme: From baseline to fifteen minutes after start of Epidural regional anesthesia
Compare the Pupil Diameter measured five seconds after time to peak of contraction before Epidural regional anesthesia and after Epidural regional anesthesia
From baseline to fifteen minutes after start of Epidural regional anesthesia
Visual Analogic Scale (VAS)
Tidsramme: From baseline to fifteen minutes after start of Epidural regional anesthesia
Compare the VAS measured at the end of contraction before Epidural regional anesthesia and after Epidural regional anesthesia.
From baseline to fifteen minutes after start of Epidural regional anesthesia

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. november 2012

Primær færdiggørelse (Faktiske)

1. marts 2013

Studieafslutning (Faktiske)

1. marts 2013

Datoer for studieregistrering

Først indsendt

11. september 2015

Først indsendt, der opfyldte QC-kriterier

15. september 2015

Først opslået (Skøn)

16. september 2015

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

16. september 2015

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

15. september 2015

Sidst verificeret

1. september 2015

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 1208078

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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