Efficacy and Satisfaction With Remifentanil Analgesia in Parturients During the Childbirth

Completed

• Conditions: Complication of Labor and/or Delivery
• Interventions: Drug: remifentanil

• Registration Number: NCT02447757
• Lead Sponsor: Brno University Hospital

Brief 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.

Detailed Description

In retrospective observational study will authors search the documentation of parturients. The cohort size is estimated to 100 subjects, in period between 2010-2014. Excluded will be all patients who did not signed the informed consent for processing with their medical data.The main aim is to evaluate the efficacy of the remifentanil analgesia in parturients in the first phase of delivery.

The analgesic efficacy will be evaluated by the change in VAS (visual analogue scale) score after induction of remifentanil analgesia Satisfaction will be evaluated by the questionary.

Study Timeline

• Study Start: 2010-01
• Primary Completion: 2015-01
• Study First Submitted: 2015-05-15
• Study First Submitted QC: 2015-05-15
• Study First Posted: 2015-05-19
• Study Completion: 2016-02
• Status Verified: 2016-07
• Last Update Submitted: 2016-07-22
• Last Update Posted: 2016-07-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 66

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Parturients with remifentanil analgesia	remifentanil	Parturients after induction of remifentanyl analgesia during the delivery

Primary Outcome Measures

Name	Time	Method
Efficacy of remifentanyl analgesia during the delivery	VAS score before the induction of remifentanyl infusion and 1hour after initiation of remifentanil analgesia during the first phase of delivery	To evaluate the efficacy of remifentanil analgesia during the first phase of delivery in parturients by observing changes in VAS score

Secondary Outcome Measures

Name	Time	Method
Patient satisfaction with analgetic method	Before initiation of anagetic method (first phase of delivery) and 1hour after childbirth	Patients will fill the questionaire to obtain their opinion on the remifentanil analgesia

Trial Locations

Locations (2)

KDAR - department of pediatrics anesthesia and resuscitation; 🇨🇿 Brno, Czech Republic

Sokolov Hospital; 🇨🇿 Sokolov, Czech Republic