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NCT05840367
Mothers' Experience of Category 1 Cesarean Section
trial testing Partner present in the operation room in Cesarean Section Complications in 15 participants. Currently enrolling.
30 November 2024
Quick facts
| Lead sponsor | Sygehus Lillebaelt |
|---|---|
| Status | Recruiting now |
| Study type | OBSERVATIONAL |
| Enrollment | 15 |
| Start date | 1 June 2023 |
| Primary completion | 30 November 2024 |
| Estimated completion | 31 December 2024 |
| Sites | 1 location across Denmark |
Drugs / interventions tested
- Partner present in the operation room
Conditions studied
- Cesarean Section Complications — all drugs for Cesarean Section Complications →
Sponsor
Sygehus Lillebaelt — full company profile →
Who can join
18 and older, female only, with Cesarean Section Complications. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The aim of this qualitative prospective study is to investigate how mothers experience a category 1 cesarean section in a hospital where the partner is present in the operation room during the entire process (induction of general anestesia, cesarean section, possible resuscitation of newborn). Mothers will be included in the study, if they wish to participate, on day 1 or 2 following the cesarean section and a brief, structured interview will be held concerning her experience of the cesarean section. Clinical baseline data regarding the mother, the cesarean section and the infant will be collected from patients files. Mothers will be contacted again three months after the cesarean section, and a semi-structured interview will be held via telephone. At the end of the interview a screening for posttraumatic stress will be performed, using the PTSD-8 tool. The interviews will be recorded and transscribed verbatim. Content of interviews will be analysed using manifest content analysis. NVivo software will be used for coding interviews.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05840367
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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Related trials
Other recruiting trials for Cesarean Section Complications
Currently open trials in the same condition.
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- NCT07130747 — Effect of Myofascial Release Versus Deep Friction Massage on Abdominal Recovery and Scar After Cesarean Section · NA · recruiting
- NCT05791630 — The Norwegian World Health Organisation Labour Care Guide Trial (NORWEL) · NA · recruiting
- NCT07049705 — Factors Influencing Bradycardia During Spinal Anesthesia in Obstetric Patients Undergoing Cesarean Section · active not 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
- NCT04948892 — Presence of the Father During Hyperacute Cesarean Section in General Anesthesia · completed
- 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 NCT05840367 (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: 26 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/NCT05840367.
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