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Intrathecal Analgesia in Laparoscopic Nissen Fundoplication.

4. juni 2026 opdateret af: Ragnar Henningsson, Karlstad Central Hospital

Intrathecal Morhine or Fentanyl Compared to Intravenous Morphine in Laparoscopic Nissen Fundoplication.

Patients planned for laparoscopic Nissen fundoplication or robotic- assisted laparoscopic surgery will receive either intrathecal morphine, intrathecal fentanyl or iv morphine (control).

Perioperative total opioid consumption, Postoperative Pain Numeric Rating scale, grade of nausea and time in the postoperative ward are compared. Total grade of patient satisfaction (0-10) as well as total hospital length are also compared.

Studieoversigt

Detaljeret beskrivelse

Study Description:

Background:

The field of laparoscopic and robotic-assisted laparoscopic surgery increases all the time. Older and more fragile patients can be suitable for laparoscopic surgery compared to open surgery, because of the less trauma and inflammatory response to the surgery and thereby faster recovery.

Extreme positioning of the patients as well as painful stimuli during and after surgery could still stress the circulatory response of the patient causing a mismatch in oxygen delivery and needs. Perioperative pain relief could be even more important during this type of surgery, when painful stimuli are more unpredictable.

This Study:

In this study painful stimuli during surgery are registered by the NOL pain monitor (Nociception Level) and intraoperative dosing of analgesia (remifentanil) is guided by the NOL index. NOL < 25 is accepted during surgery.

All patients receive preoperative: Acetaminophen 1g, Meclozinehydrocloride 25mg.

• Total opioid consumption during and after surgery is compared between three groups of patients receiving: Patients receiving Fentanyl intrathecal need 6 hours postoperative observation and patients receiving morphine intrathecal need 10 hours observation time.

  1. Preoperative: Oxycodone orally
  2. Preoperative: Intrathecal Fentanyl
  3. Preoperative Intrathecal Morphine. Preoperative pain assessment of the patients are Postoperative Pain from Assessment of Pain Associated with Venous Cannulation (1-10)

Anesthesia: Induction of anesthesia with propofol, remifentanil and rocuronium. During surgery: Sevoflurane + remifentanil. BIS 35-50. NOL <25. Monitoring: EKG, Blood pressure, BIS (Bispectral index) and NOL. Before wake up: Parecoxib 40mg iv. Ondansetron 4mg iv. Group 1: Morphine 0,05mg/kg iv. 10 min before waking up: 1ug/kg fentanyl to all patients. Time of surgery is also registered and volume of bleeding as well.

After surgery:

NRS (Numeric Pain Scores (0-10) are registered in the PAVU when the patient is at the PACU, when leaving the PACU as well as the maximum pain score postoperative.

Total dose of opioids converted to morphine equivalents are compared between the groups as well as the pain scores and time in the PACU.

Power calculation show a need for 63 patients to receive 80% power to show a difference in morphine-equivalents between groups of 1 mgs. (p<0,05).

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

63

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiesteder

    • Värmland County
      • Karlstad, Värmland County, Sverige, 65229
        • Department of Anesthesia & Intensive Care, Central Hospital of Karlstad

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

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria: All patients scheduled for laparoscopic fundoplicatio surgery

-

Exclusion Criteria: -

  • Age < 18 years
  • Chronic pain problems or abuse.
  • Pregnancy
  • Exclusion ciriteria for spinal anesthesia.

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Støttende pleje
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Intrathecal Fentanyl 20ug
Preoperative spinal with 20ug Fentanyl
Intrathecal Fentanyl
Aktiv komparator: Intrathecal Morphine 100ug
Preoperative Spinal with 100ug Morhine.
Norhine 100ug intrathecal
Andre navne:
  • Morphine 100ug intrathecal
Andet: Intravenous Morphine analgesia
NOL- guided Intravenous Morphine analgesia
NOL guided intravenous morphine analgesia
Andre navne:
  • Styring
  • intravenous morphine

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Three different treatments of pain during during laparoscopic and/or robotic assisted laparoscopic Nissen fundoplication.
Tidsramme: From enrollment to the end of treatment - usually the day after surgery.
  1. Primary outcome measure: Total perioperative opioid consumtion converted to morphine equivalents.
  2. Secondary outcome measure: Patient pain scores (NRS 1-10) when arriving at the PACU, when leaving the PACU and the highest pain score in the PACU.
From enrollment to the end of treatment - usually the day after surgery.
Postoperative pain assessed using the Visual Analogue Scale (VAS) upon arrival to the post-anesthesia care unit (PACU), maximum VAS score in PACU, and at discharge to ward/home/patient hotel.
Tidsramme: From inclusion to the day after surgery.

Secondary outcomes:

  1. Total intraoperative opioid dose and postoperative opioid and other analgesic requirements during the first 24 hours.
  2. Postoperative nausea (0-10 scale).
  3. Need for antiemetic treatment postoperatively. Length of hospital stay (days).

8. Need for urinary catheterization (indwelling catheter or intermittent catheterization) within 24 hours postoperatively or at discharge.

From inclusion to the day after surgery.
"Number of Participants with Treatment-Related Adverse Events as Assessed by CTCAE v4.0"
Tidsramme: "From enrollment to the end of treatment at the day after surgery
Paricipants arriving at the PACU with pain score according to the Visual Analogue Scale (VAS) > 3
"From enrollment to the end of treatment at the day after surgery

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 (Faktiske)

10. marts 2026

Primær færdiggørelse (Anslået)

31. december 2026

Studieafslutning (Anslået)

31. marts 2027

Datoer for studieregistrering

Først indsendt

10. marts 2026

Først indsendt, der opfyldte QC-kriterier

4. juni 2026

Først opslået (Faktiske)

5. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

5. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

4. juni 2026

Sidst verificeret

1. juni 2026

Mere information

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Studerer et amerikansk FDA-reguleret enhedsprodukt

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