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Klonidin as pain relief in eye examination of premature infants - cloROP

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-512438-14-00
Enrollment
50
Registered
2024-07-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Pain during eye examination of premature infants.

Brief summary

PIPP-R scores within 30 seconds after the eye examination has been initiated, i.e. when the hooks are in place in the first eye in Uppsala or when the first eye is held open in Örebro.

Detailed description

GSR: Area small peaks, area huge peaks, peaks per second och average rise time, Number of reported AEs, SAEs and SUSARS, A VAS scale of 0-10 cm, from very easy to examin (0) to very difficult to examin (10)

Interventions

DRUGCLONIDINE

Sponsors

Region Oerebro Laen
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
0 Years to 17 Years

Design outcomes

Primary

MeasureTime frame
PIPP-R scores within 30 seconds after the eye examination has been initiated, i.e. when the hooks are in place in the first eye in Uppsala or when the first eye is held open in Örebro.

Secondary

MeasureTime frame
GSR: Area small peaks, area huge peaks, peaks per second och average rise time, Number of reported AEs, SAEs and SUSARS, A VAS scale of 0-10 cm, from very easy to examin (0) to very difficult to examin (10)

Countries

Sweden

Outcome results

None listed

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