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DAY-HEP

Feasibility of Same-Day Discharge After Robot Assisted Liver Surgery - DAY-HEP

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON58071
Enrollment
30
Registered
2025-07-02
Start date
2026-01-09
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignancy, cancer, carcinoma, hepatocarcinoma, liver cancer, metastasis Cancer, colon cancer, liver cancer, metastasis

Interventions

Sponsors

OLVG
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Anticipated minor or technically major liver resection (less than 3 bordering anterolateral (2,3,4b,5 and 6 or posterior-superior (1,4a,7 and 8) segments)Procedure not combined with microwave ablationNo simultanious colon resectionNo usage of anticoagulantsASA Classification I or IIPatient is able to use an ear thermometer and pulse-oxymeterPatient has an informal caregiver (e.g. partner, family member, friend) present for the first 24 hours after surgeryPatient resides within a 45-minute drive from the OLVG Hospital

Exclusion criteria

Exclusion criteria: Patients younger than 18 years oldPatient does not wish to undergo SDDSecondary exclusion criteriaResection is more extensive than anticipated (major liver resection, i.e. > 3 bordering anatomical segments resected)Intraoperative blood loss exceeding 500ccOperating time exceeds 4 hoursBile leakage or risk of postoperative haemorrhage necessitating postoperative drainage or anesthesiological complications.Abnormal vital signs (tachycardia >100, temperature above 38.4 Celsius, hypotension at the end of the afternoon) or drop in Hemoglobin level >1 point 6 hours postoperativelyPostoperative vomiting, wound problems, excess pain, or other causes of doubt.

Design outcomes

Primary

MeasureTime frame
In this present study the primary outcome is the percentage of successful SDD with usage of remote monitoring. Successful SDD was defined as SDD without readmission within 48 hours. This endpoint is chosen to assess the feasibility of the concept in current practice. SDD is considered feasible if >75% successful SDD can be applied in the selected patient group.

Secondary

MeasureTime frame
To obtain information about the safety of SDD and remote monitoring of the selected group of patients undergoing hepatic surgery we will analyse adverse outcomes including complications ranked in the Clavien-Dindo classification, emergency room presentations, readmissions, reoperations and mortality. Furthermore, monitoring of time to detection of the complication and prompt treatment is necessary as these factors contribute to the patient’s outcome. We will evaluate patient satisfaction and experience with the hospital care around SDD by using the QoR-15 Patient Survey. The questionnaire will be given to patients after the operation, this composed questionnaire consisting of two sections, involving 10-point Likert scale questions. The QoR-15 Patient survey is a validated and efficient measurement of postoperative recovery.

Countries

Netherlands

Contacts

Public ContactB.W. Verboeket

OLVG

b.w.verboeket@olvg.nl0657568110

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Feb 3, 2026