Efficacy and Satisfaction With Remifentanil Analgesia in Parturients During the Childbirth

Efficacy and Satisfaction With Remifentanil Analgesia in Parturients During the Childbirth: Retrospective Observational Study

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02447757

Enrollment

Registered

2015-05-19

Start date

2010-01-31

Completion date

2016-02-29

Last updated

2016-07-26

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

Conditions

Complication of Labor and/or Delivery

Keywords

Remifentanil, delivery, childbirth, analgesia, parturition, confinement

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.

Interventions

DRUGremifentanil

Remifentanil analgesia during delivery

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 50 Years

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame	Description
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

Measure	Time frame	Description
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

Countries

Czechia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026