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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04948892
Other study ID # SC210815
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date October 1, 2023

Study information

Verified date April 2024
Source Sygehus Lillebaelt
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study concerns cesarean sections, category 1, meaning those cases where the life of mother and/or fetus is in immedeate danger and the child must be delivered within 15 minutes from activating the cesarean section team. In most hospitals in Denmark, these cesarean sections are most often performed in general anesthesia and the mother is endotracheally intubated. Previously in these situations, as the mother was rushed from the Labour Ward to the operation room (OR), her spouse/partner, would be placed outside the operating room (OR), and would stay there until the child had been delivered. In Lillebaelt Hospital, Kolding, Denmark, the newborn-resuscitation table is placed inside the OR. The father would most often be allowed to enter the OR when the child was delivered and placed on the resuscitation table (no matter the status of the child). However, during spring 2021, Lillebaelt Hospital Kolding updated the policy regarding the handling of the father/partner during cesarean section category 1. Now the father/partner is present in the OR during the whole procedure, including induction of general aesthesia, endotracheal intubation, performance of the cesarean section (drapings are positioned so that the father cannot see the operation field) and potential resuscitation efforts of the newborn. In another hospital in the same region (Region of Southern Denmark), Aabenraa Hospital, the father is not present in the OR during the cesarean section. He waits in the labour ward. The investigators therefore wish to investigate how the cesarean section category 1 is experienced by: the father/partner; the mother; the obstetrician; the anestesiologist; the midwife; the OR nurse; the anesthetic nurse, both in Kolding where the father/partner is present in the OR, and in Aabenraa, where the father/partner is not present in the OR during the cesarean sectio.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date October 1, 2023
Est. primary completion date January 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - cesarean section category 1 Exclusion Criteria: - none

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Prescence of the father during cesarean section in general anesthesia
The father is now present in the OR during cesarean section category 1, instead of waiting outside

Locations

Country Name City State
Denmark Aabenraa Hospital Aabenraa
Denmark Helene K. Nedergaard Kolding

Sponsors (1)

Lead Sponsor Collaborator
Sygehus Lillebaelt

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Obstetric complications Perforation of bladder or bowel, bleeding > 1000 ml, infection, need for transfusion Up to 1 week after the cesarean section
Other Anesthetic complications Esophageal intubation, difficult airway management During cesarean section
Other Neonatal complications Low APGAR-score, need for resuscitation, need for intubation, need for transfusion During cesarean section
Primary Father/partners experience Father/partners experience of being present or not in the OR during the hyperacute cesarean section category 1, described by questionnaire, semi-structured interview and PTSD-screening 1-2 days after the cesarean section combined with assessment of change from baseline in father/partners experience at 3 months after the cesarean sectio
Secondary Mothers experience Mothers experience of the father/partner being present or not in the OR during the hyperacute cesarean section category 1, described quantitatively with possibility for qualitative components 1-2 days after the cesarean section
Secondary Surgeons (obstetricians) experience Surgeons experience of the father/partner being present or not in the OR during the hyperacute cesarean section category 1, described quantitatively with possibility for qualitative components Up to 2 weeks after the cesarean section
Secondary Anesthesiologists experience Anesthesiologists experience of the father/partner being present or not in the OR during the hyperacute cesarean section category 1, described quantitatively with possibility for qualitative components Up to 2 weeks after the cesarean section
Secondary Midwifes experience Midwifes experience of the father/partner being present or not in the OR during the acute cesarean section category 1, described quantitatively with possibility for qualitative components Up to 2 weeks after the cesarean section
Secondary OR nurses experience OR nurses experience of the father being present or not in the OR during the hyperacute cesarean section category 1, described quantitatively with possibility for qualitative components Up to 2 weeks after the cesarean section
Secondary Anesthetic nurses experience Anesthetic nurses experience of the father/partner being present or not in the OR during the hyperacute cesarean section category 1, described quantitatively with possibility for qualitative components Up to 2 weeks after the cesarean section
Secondary Pediatricians experience Pediatricians experience of the father/partner being present or not in the OR during the hyperacute cesarean section category 1, described quantitatively with possibility for qualitative components Up to 2 weeks after the cesarean section
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