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NCT04142203: Herko
Implementation of 23 Hour Surgery Model in a Tertiary Hospital
trial testing 23 h surgery in Ambulatory Surgery in 993 participants. Completed in 30 May 2021.
30 May 2021
Quick facts
| Lead sponsor | Kuopio University Hospital |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 993 |
| Start date | 16 May 2017 |
| Primary completion | 30 May 2021 |
| Estimated completion | 30 May 2021 |
| Sites | 1 location across Finland |
Drugs / interventions tested
- 23 h surgery
Conditions studied
- Ambulatory Surgery — all drugs for Ambulatory Surgery →
- Laparoscopy — all drugs for Laparoscopy →
- Shoulder Impingement Syndrome — all drugs for Shoulder Impingement Syndrome →
- Ovarian Cysts — all drugs for Ovarian Cysts →
Sponsor
Kuopio University Hospital
Who can join
Adults 18 to 100, any sex, with Ambulatory Surgery or Laparoscopy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Extended day surgery or 23 h surgery (23-hour surgery) is a surgical model where patients arrive to the hospital from home at the day of surgery, are operated and recover in a 23 h surgery unit. 23H surgery units are usually situated near postoperative recovery unit. THe 23 H surgical model was implemented in Kuopio University Hospital 2015 and between May 2017-May 2018 patients were recruited in the present prospective follow up cohort study. Patients were informed and they gave their informed consent. The patients were contacted two weeks after the study and details of their recovery were asked.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
Resilience, pain, and health-related quality of life in gynecological patients undergoing surgery for benign and malignant conditions: a 12-month follow-up study.
Isokääntä S, Ruohoaho UM, Anttila M, Kokki H, et al · · 2022 · cited 7× · PMID 35974326 · DOI 10.1186/s12905-022-01923-7 -
Implementation of a 23-h surgery model in a tertiary care hospital: a safe and feasible model with high patient satisfaction.
Ruohoaho UM, Toroi P, Hirvonen J, Aaltomaa S, et al · · 2020 · cited 6× · PMID 32109004 · DOI 10.1002/bjs5.50267 -
Patient functional recovery after a 23-h surgery - a prospective, follow-up study.
Ruohoaho UM, Aaltomaa S, Kokki H, Anttila M, et al · · 2022 · PMID 35384504 · DOI 10.1007/s00423-022-02502-y
Verify or expand the search:
- PubMed search for NCT04142203
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Other Kuopio University Hospital trials
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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 NCT04142203 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Kuopio University Hospital
- Last refreshed: 12 April 2022
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/NCT04142203.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing