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NCT Number: NCT02447757

Efficacy and Satisfaction With Remifentanil Analgesia in Parturients During the Childbirth

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.

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Key information

Conditions

Complication of Labor and/or Delivery Agnosia Nervous System Diseases Neurobehavioral Manifestations Neurologic Manifestations Pathological Conditions, Signs and Symptoms Perceptual Disorders Signs and Symptoms

Age range

18 year–50 year

Sex eligibility

Female

Study type

Observational

Primary location

KDAR - department of pediatrics anesthesia and resuscitation, Brno, Czechia

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

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

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

Treatment and study plan

Remifentanil

Drug

Remifentanil analgesia during delivery

Primary outcomes

  1. Efficacy of remifentanyl analgesia during the delivery

    Time frame: 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 outcomes

  1. Patient satisfaction with analgetic method

    Time frame: 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

Sponsors and collaborators

Lead sponsor

Brno University Hospital

Other

Collaborators

  • Hospital Sokolov

Registry information

Official study title

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

Important dates

Study start
2010
Primary completion
2015
Study completion
2016
First posted
May 19, 2015
Registry last updated
Jul 26, 2016

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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