Continuous vs. Bolus Administration of NSAIDs After Laparoscopic Surgery for Multimodal Analgesia

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorFederal Research and Clinical Centre of Intensive Care Medicine and Rehabilitology

About this trial

Currently the prevalent approach to perioperative management of patients is ERAS (Enhanced Recovery After Surgery) concept. This approach includes numerous aspects, among which the perioperative use of multimodal analgesia takes one of the leading places. Within the ERAS guidelines all sorts of minimization of opioid analgesics use in schemes of postoperative analgesia are appreciated. Thus, new pharmacological approaches are being actively developed currently in order to achieve adequate analgesia and to minimize the use of this group of drugs.

One of the most perspective trends within the multimodal analgesia concept is continuous infusion of non-steroidal anti-inflammatory drugs (NSAID). Up to date there are papers that both confirm the effectiveness of this method for maintaining adequate postoperative analgesia and show its limitations and deny the advantages of the continuous use of NSAID.

Up to this time the main attention of the medical community was paid for such drugs as paracetamol and ketoprofen. Nevertheless, one of the most common and safe NSAID is ibuprofen. In spite of this, there are no studies that explore the effectiveness of the continuous infusion of this drug. Thus, the lack of even low-quality evidence led to setting up a study of effectiveness and safety of continuous infusion of ibuprofen in comparison to its bolus injection.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age > 18 years old

Elective laparoscopic surgery

General anesthesia

Signed informed consent from the patient to participate in the study

Disqualifiers

History of ibuprofen allergy

Active erosive or ulcerative lesions of the gastrointestinal tract

Chronic use of opioid analgesics or NSAIDs prior to enrollment

Chronic kidney disease ≥ 3b stage according to the KDIGO classification

Trial design

Design model

Parallel

Treatments tested in this trial

  • Ibuprofen continuous infusion

    Drug

    1. The first bolus: ibuprofen 400 mg diluted in 0,9% NaCl 200 ml is intravenous injected during the first hour right after the admission to the department. The drug is injected during the first hour at the rate of 4 mg/kg/h for the ideal body weight. 2. Continuous infusion: * Ibuprofen 1200 mg diluted in 0,9% NaCl 300 ml is intravenous injected on the first day with the speed of 1 mg/kg/h (for the ideal body weight) during the remaining 23 hours. * On the second day the intravenous infusion of ibuprofen 1600 mg diluted in 0,9% NaCl 400 ml with the speed of 1 mg/kg/h is continued during the 24 hours. 3. Imitation of bolus: Every 8 hours placebo (0, 9% NaCl 200 ml) is intravenous injected to create an imitation of bolus injection. Placebo is injected during the first hour.

  • Ibuprofen bolus injection

    Drug

    1. The first bolus: ibuprofen 400 mg diluted in 0, 9% NaCl 200 ml is intravenous injected during the first hour right after the admission to the department. The drug is injected during the first hour at the rate of 4 mg/kg/h for the ideal body weight. 2. Bolus injection: * Every 8 hours a intravenous bolus of ibuprofen 800 mg diluted in 0,9% NaCl 200 ml is injected during 1 hour (3 boluses per day in total). * On the second day the every 8 hours intravenous bolus of ibuprofen 800 mg diluted in 0, 9% NaCl 200 ml is injected during 1 hour (3 boluses per day in total). 3. Placebo continuous infusion: Between the boluses a placebo (0,9% NaCl) continuous intravenous infusion is performed with the speed imitating the speed of ibuprofen infusion in the experimental group.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: NSAID bolus injectionActive comparator 1 intervention
Group B: NSAID continuous infusionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Opioid consumption

Evaluation of the overall consumption of opioid analgesics after surgery during the whole postoperative period

Time frame
up to 28 days

Secondary outcomes

1

Pain intensity assessment

Evaluation of postoperative pain intensity using the Numerical Rating Scale (NRS); measurements at regular intervals and before rescue analgesia if pain exceeds NRS \>5. The maximum value is 10, the minimum value is 0. The higher the value, the more severe patient's pain (worse).

Time frame
From admission to ICU until 48 hours postoperatively

Other outcomes

1

NSAID-related Adverse Effects

Incidence and severity of adverse effects including respiratory depression, gastrointestinal dysfunction, hepatotoxicity, renal dysfunction, allergic reactions, and CNS effects.

Time frame
up to 28 days
2

Length of ICU stay

The number of days between the day of discharge from the ICU (or in-hospital death) after initial admission and the day of randomization.

Time frame
1 year
3

Length of Hospital Stay

The number of days between the day of discharge from the hospital (or in-hospital death) after initial admission and the day of randomization.

Time frame
1 year
4

ICU Readmission

Incidence of readmission to the intensive care unit within 28 days from the day of randomization.

Time frame
Within 28 days from randomization

Locations

1

Map coordinates are unavailable for these locations. Locations are shown below instead.

City Clinical Hospital named after S.S. YudinRecruiting115446, Moscow, Moscow OblastRussiaRussia

Sponsors and contacts

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