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Longterm follow-up of a controlled randomized trial of single-port laparoscopic cholecystecomy vs. multiport laparoscopic cholecystecomy

Longterm follow-up of a controlled randomized trial of single-port laparoscopic cholecystecomy vs. multiport laparoscopic cholecystecomy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00012447
Enrollment
200
Registered
2017-05-12
Start date
2017-04-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

K80

Interventions

Group 1: Single-port laparoscopic cholecystectomy Group 2: Multiport laparoscopic cholecystectomy

Sponsors

Charité Campus Charité Mitte
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Colecystectomy as primary operation, Patients older than 18 years od Age, Participation of the previous controlled randomized trial comparing the single-port and multiport laparoscopic cholecystectomy.

Exclusion criteria

Exclusion criteria: Not self-sufficient patients, patients under 18 years, patient's desire

Design outcomes

Primary

MeasureTime frame
No difference in rates of incisional hernias between single-port and multiport laparoscopic cholecystectomy. A single clinical and sonographic check of the operated patients is performed.

Secondary

MeasureTime frame
No difference in scar cosmetic outcome between single-port and multiport laparoscopic cholecystectomy

Countries

Germany

Contacts

Public ContactJonas Raakow

Charité Campus Charité Mitte

jonas.raakow@charite.de030450522012

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 18, 2026