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NCT04948892
Presence of the Father During Hyperacute Cesarean Section in General Anesthesia
trial testing Prescence of the father during cesarean section in general anesthesia in Cesarean Section in 26 participants. Completed in 1 October 2023.
1 January 2023
Quick facts
| Lead sponsor | Sygehus Lillebaelt |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 26 |
| Start date | 1 January 2022 |
| Primary completion | 1 January 2023 |
| Estimated completion | 1 October 2023 |
| Sites | 2 locations across Denmark |
Drugs / interventions tested
- Prescence of the father during cesarean section in general anesthesia
Conditions studied
- Cesarean Section — all drugs for Cesarean Section →
Sponsor
Sygehus Lillebaelt — full company profile →
Who can join
18 and older, any sex, with Cesarean Section. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04948892
- Europe PMC full search
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Related trials
Other recruiting trials for Cesarean Section
Currently open trials in the same condition.
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- NCT07413185 — Relationship Between the Severity of Sleep Deprivation in the First 48 Hours Postpartum, Breastfeeding Motivation, and B · recruiting
- NCT07440667 — Restrictive vs Liberal Intraoperative Fluid Strategy and Postoperative Outcomes After Elective Cesarean Section · NA · recruiting
Other Sygehus Lillebaelt trials
Trials by the same sponsor.
- NCT07134179 — Insufficient Regional Anesthesia for Cesarean Section: Mothers' Experiences A Qualitative Study · not yet recruiting
- NCT06669156 — Insufficient Regional Anesthesia and Conversion to General Anesthesia for Cesarean Section A Qualitative Multicenter Stu · recruiting
- NCT05933993 — Mothers Experience of Pain Following Elective Cesarean Section. A Qualitative Study. · completed
- NCT05840367 — Mothers' Experience of Category 1 Cesarean Section · recruiting
- NCT04458038 — Does Chronic Obstructive Lung Disease Influence the Cognitive Function · NA · unknown
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04948892 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sygehus Lillebaelt
- Last refreshed: 25 April 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04948892.
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