The Long-term Effect of Marine Omega-3 Fatty Acid Supplementation in Renal Transplantation

NCT03018041 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 174

Last updated 2025-04-03

No results posted yet for this study

Summary

This is a long-term intervention study on the effects of marine n-3 PUFAs in renal transplantation. Our hypothesis is that patients treated with marine n-3 PUFA supplementation will have less decline in kidney transplant function compared to patients treated with placebo.

Conditions

  • Kidney Transplantation

Interventions

DRUG

Omacor

As described in "Arms".

DRUG

Placebo Oral Capsule

As described in "Arms".

Sponsors & Collaborators

  • University of Oslo

    collaborator OTHER
  • Rikshospitalet University Hospital

    collaborator OTHER
  • Ullevaal University Hospital

    collaborator OTHER
  • Drammen sykehus

    collaborator OTHER
  • Elverum Hospital

    collaborator UNKNOWN
  • South-Eastern Norway Regional Health Authority

    collaborator OTHER
  • Aalborg University Hospital

    collaborator OTHER
  • Pronova BioPharma

    collaborator INDUSTRY
  • Haukeland University Hospital

    collaborator OTHER
  • University Hospital of North Norway

    collaborator OTHER
  • Joe Chan

    lead OTHER

Principal Investigators

  • My Svensson, MD, PhD · University Hospital, Akershus

  • Ivar Anders Eide, MD, PhD · University Hospital, Akershus

  • Branimir Draganov, MD · Ullevaal University Hospital

  • Joe Chan, MD · University Hospital, Akershus

  • Morten Reier-Nilsen, MD · Drammen sykehus

  • Tone Granseth, MD · Elverum Hospital

  • Nanna von der Lippe, MD, PhD · Ullevaal University Hospital

  • Bård Endre Waldum-Grevbo, MD, PhD · Ullevaal University Hospital

  • Per Olav Rui, MD · Haukeland University Hospital

  • Toralf Melsom, MD, PhD · University Hospital of North Norway

  • Renathe Rismo, MD, PhD · University Hospital of North Norway

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-09-01
Primary Completion
2024-03-22
Completion
2025-03-22

Countries

  • Norway

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 NCT03018041 on ClinicalTrials.gov