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Intrathecal Analgesia in Laparoscopic Nissen Fundoplication.

NCT07629323 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 63

Last updated 2026-06-05

No results posted yet for this study

Summary

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.

Conditions

  • Perioperative Pain Management
  • Gastreoesophageal Reflux Disease

Interventions

PROCEDURE

Fentanyl Intrathecal 20ug

Intrathecal Fentanyl

OTHER

NOL-guided intravenous morphine analgesia

NOL guided intravenous morphine analgesia

DRUG

Intrathecal Morphine 100ug

Norhine 100ug intrathecal

Sponsors & Collaborators

  • Karlstad Central Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-10
Primary Completion
2026-12-31
Completion
2027-03-31

Countries

  • Sweden

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07629323 on ClinicalTrials.gov