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NCT05396430
Duration of Urinary Catheter Treatment After Cesarean Delivery Under Spinal Anesthesia
NA trial testing Urinary catheter in Urinary Retention in 150 participants. Status unknown.
31 August 2023
Quick facts
| Lead sponsor | Women's Hospital HUS |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 150 |
| Start date | 1 January 2023 |
| Primary completion | 31 August 2023 |
| Estimated completion | 31 August 2023 |
| Sites | 1 location across Finland |
Drugs / interventions tested
- Urinary catheter
Conditions studied
- Urinary Retention — all drugs for Urinary Retention →
- Cesarean Section Complications — all drugs for Cesarean Section Complications →
Sponsor
Women's Hospital HUS
Who can join
Adults 18 to 55, female only, with Urinary Retention or Cesarean Section Complications. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
In this study a total of 150 parturients undergoing cesarean delivery under spinal anesthesia will be randomized to have their urinary catheters kept in place for 8, 10 or 12 hours. The incidence of urinary retention and interventions needed for any potential urinary retention will be assessed.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05396430
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Urinary catheter
Trials testing the same drug.
- NCT05643807 — Bladder Washing Cytology for Detection of Urothelial Carcinoma Using Catheter or Flexible Cystoscope: Which is Better? · NA · unknown
Other recruiting trials for Urinary Retention
Currently open trials in the same condition.
- NCT07372547 — Effect of Voiding Position (Standing in the Shower vs. Sitting) on Post-Void Residual Urine Volume (PVR) After Removal o · NA · recruiting
- NCT07355803 — Define Final Selection Choice Criteria for a Coloplast Catheter Ensuring Highest Patient Satisfaction Via Surveys (EVA). · NA · recruiting
- NCT06978205 — Effect of Urethral Balloon Dilatation on Urinary Retention After Spinal Cord Injury · NA · recruiting
- NCT06163469 — Effect of Chlorhexidine Gluconate Bladder Instillations in Patients With Chronic Suprapubic Catheters on Unplanned Healt · NA · recruiting
- NCT06179654 — Preoperative Pelvic Floor Physical Therapy to Minimize Stress Urinary Incontinence After Holmium Laser Enucleation of th · NA · recruiting
Other Women's Hospital HUS trials
Trials by the same sponsor.
- NCT05396378 — Early Recovery After Cesarean Delivery - Maternal Glucose Homeostasis Following Preoperative Glucose Dose · unknown
- NCT05396417 — How Well do the Current Cesarean Deliveries Adhere to the Published ERAS Guidelines? · unknown
- NCT04645823 — Spinal Fentanyl or Epidural Analgesia in the Early First Phase of Induced Labor · Phase 4 · completed
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 NCT05396430 (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 Women's Hospital HUS
- Last refreshed: 26 April 2023
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/NCT05396430.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing