CompletedPhase 4ketamine

Anesthesia for Retinopathy of Prematurity

Sponsored by TC Erciyes University

NCT ID
NCT01955135
Target Enrollment
60 participants
Start Date
2010-09
Est. Completion
2013-03

About This Study

Premature infants experience more respiratory problems after surgical procedures. The investigators aimed to compare general anesthesia with sedation on the need for post-operative mechanical ventilation in infants undergoing retinopathy of prematurity surgery.

Conditions Studied

Retinopathy

Interventions

  • Ketamine
  • Sevoflurane
  • propofol

Eligibility

Age:32 Weeks - 40 Weeks
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* infants aged 32-40 weeks who were scheduled to undergo laser surgery for treatment of ROP

Exclusion Criteria:

* The exclusion criteria were patients requiring inotropic support,
* the need for mechanical ventilation or intubation in the 3 days prior to the operation,
* known allergy or hypersensitivity reaction to ketamine and propofol,
* age ˃40 weeks.

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source