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Paxlovid long covid-19 prevention trial with recruitment in the community in Norway

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-510337-29-00
Acronym
PANORAMIC-Norway
Enrollment
2000
Registered
2024-06-24
Start date
2023-04-11
Completion date
Unknown
Last updated
2025-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Virus Diseases

Brief summary

Continued symptoms of acute COVID-19 and new symptoms according to long-COVID illness.

Detailed description

A cause, non-elective hospitalisation and/or death, within 28 days of randomisation., Participant reported symptoms daily for 7 days, weekly for 28 days and at 3 and 6 months., Contacts with health services reported by paticipants and/or captured by review for health registries., New infections in the household reported by the participants., Evaluation of overall safety of drugs by the monitoring of adverse events (AEs as defined in the ISAs)., Well-being, symptoms and health care utilisation., Resource use and cost data.

Interventions

DRUGRITONAVIR
DRUGPlacebo: Round
DRUGwhite tablet with breakmarks on one side
DRUGno imprints 8 x 8 mm; Maydis amylum 10%
DRUGCellulosum microcrist. 89%
DRUGMagnesii stearas 0
DRUG5% and Silica colloid. anhydr. 0
DRUG5%

Sponsors

Helse Bergen HF
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Continued symptoms of acute COVID-19 and new symptoms according to long-COVID illness.

Secondary

MeasureTime frame
A cause, non-elective hospitalisation and/or death, within 28 days of randomisation., Participant reported symptoms daily for 7 days, weekly for 28 days and at 3 and 6 months., Contacts with health services reported by paticipants and/or captured by review for health registries., New infections in the household reported by the participants., Evaluation of overall safety of drugs by the monitoring of adverse events (AEs as defined in the ISAs)., Well-being, symptoms and health care utilisation., Resource use and cost data.

Countries

Norway

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026