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OpenTrials
Completed

NCT Number: NCT00386269

Double Blind Randomized Study Into the Efficacy of Codeine Phosphate Analgesia After Cleft Palate Repair in Infants

This study examines the analgesic efficacy of codeine phosphate. It is compared to placebo in infants receiving morphine after surgery. Codeine may be effective enough to make morphine unnecessary.

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Key information

Conditions

Cleft Palate Repair

Age range

4 month–8 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Great Ormond Street Hospital, Anaesthetics

London, WC1N 1EH, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Infants with cleft palate

Treatment and study plan

Codeine Phosphate Analgesia

Drug

Primary outcomes

  1. Dose of morphine used within the first 6h after surgery

Secondary outcomes

  1. Pain scores

Sponsors and collaborators

Lead sponsor

Institute of Child Health

Other

Registry information

Important dates

Study start
2004
Study completion
2007
First posted
Oct 11, 2006
Registry last updated
Nov 29, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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