Efficacy and Satisfaction With Remifentanil Analgesia in Parturients During the Childbirth

• Status: Completed
• Trial end date: 2016-02-01
• Target enrollment: 0
• Participant gender: Female

Summary

Retrospective observational study to determine the efficacy of remifentanil during the delivery. Authors will search the data in period between 2010 and 2014 in cohort of 100 parturients and obtain data of analgesic efficacy (VAS score after remifentanil analgesia induction) and parturients satisfaction with the method.

• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Brno University Hospital
• Collaborator: Hospital Sokolov
• Treatments: Remifentanil

Criteria

Inclusion Criteria:

• parturients during the delivery

• administered remifentanil analgesia

• signed informed consent

Exclusion Criteria:

• informed consent not signed

• missing data about the analgetic method a analgetic efficacy