Case-control study single port cholecystectomy versus conventional cholecystectomy

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00003122

Enrollment

200

Registered

2011-09-12

Start date

2009-01-01

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

Complications following laparoscopic cholecystectomy K80.20

Interventions

Group 1: Single Port Cholecystectomy Group 2: Conventional Laparoscopic Cholecystectomy

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: chronic and acute cholecystolithiasis

Exclusion criteria

Exclusion criteria: previous laparotomies, liver cirrhosis

Design outcomes

Primary

Measure	Time frame
Primary endpoint is the postoperative complication rate. The complication rate is evaluated in the postoperative hospital stay.	—

Secondary

Measure	Time frame
cosmetic results	—

Countries

Germany

Contacts

Public ContactErnst Hanisch

Asklepios Klinik Langen Akademisches Lehrkrankenhaus Goethe-Universität Frankfurt

e.hanisch@asklepios.com06103 912 1309

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026