Long-term outcome of Quality of Life and Symptom Control after participation on the trial: Robotic versus Conventional laparoscopic fundoplication (ROLAF) Trial

Long-term outcome of Quality of Life and Symptom Control after participation on the trial: Robotic versus Conventional laparoscopic fundoplication (ROLAF) Trial - ROLAF

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00014690

Enrollment

Registered

2018-06-12

Start date

2018-06-17

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

K21

Interventions

Group 1: Quality of Life follow-up of patients who underwent laparoscopic Nissen fundoplication by validated questionnaires. Group 2: Quality of Life follow-up of patients who underwent robotic-assis

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Initial participation in the ROLAF trial, comparing robotic-assisted versus laparoscopic fundoplication.

Exclusion criteria

Exclusion criteria: No participation on the ROLAF Trial.

Design outcomes

Primary

Measure	Time frame
- Quality Of Life in Reflux and Dyspepsia (QOLRAD) (Questionnaire) - 10 years after initial procedure	—

Secondary

Measure	Time frame
- Gastrointestinal Symptom Rating Sclae (GSRS) (Questionnaire) - 10 years after initial procedure	—

Countries

Germany

Contacts

Public ContactFelix Nickel

Universitätsklinikum Heidelberg

felix.nickel@med.uni-heidelberg.de+496221-568641

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 19, 2026