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Evaluation of the Effect the Medical Team in the Delivery Room Has on Pain Management During Labor.

Labor Pain Clinical Trial

Official title:
Evaluation of the Effect the Medical Team in the Delivery Room Has on Pain Management During Labor.

Clinical Trial Summary

In the current study the investigators wish to evaluate the effect the doctors and midwives in the delivery room have on the timing and modality of analgesia chosen by the participants. The participants will be randomly divided into 2 groups. Both groups will be advised of the different modalities of analgesia available during labor. One group will be managed in the delivery room the same as if not part of the study, meaning the doctors and midwives will treat the participants the way they usually do regarding analgesia. The second group of participants will not be asked by the doctors and midwives about analgesia at all but will be able to receive analgesia by a modality of choice at the timing of choice.

Clinical Trial Description

After explaining to the participants the study and having signed a confirmed consent, participants will receive an extensive explanation regarding the different modalities of analgesia available during labor. After the explanations the participants will be randomly divided into 2 groups:

1. Routine management-doctors and midwives will treat the participants the way they usually do regarding analgesia including frequent inquiries about wishes for analgesia.

2. Interventional management-participants will not be asked by the doctors and midwives about analgesia at all during labor but will be able to receive analgesia by a modality of choice at the timing of choice after being advised by the medical team.

After delivery, participants will fill a questionnaire regarding the experience of labor in general and the relevance of analgesia during labor including the effect the medical team may have had on decision making during labor.

Medical information regarding visual analogue scale (VAS), analgesia modality, cervical conditions, parity etc. will be extracted from patients' electronic files. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03045705
Study type Interventional
Source Rambam Health Care Campus
Contact
Status Withdrawn
Phase N/A
Start date March 1, 2019
Completion date September 1, 2020
View Details
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