Recruiting NCT03326154
Post-Cholecystectomy Quality of Life
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: No intervention, observational.
- Who it may be relevant to
- Registry conditions: Gallstone. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Finland
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Health Related Quality of Life and Abdominal Symptoms After Cholecystectomy
Overview
The study aims to identify factors associated with no increase in gastrointestinal quality of life after elective cholecystectomy for gallstones.
Interventions
- Other No intervention, observational
Observation
Primary outcome measures
- Quality of life: Gastrointestinal Quality of Life GIQLI score [Time frame: 1 year]
Eligibility criteria
Inclusion criteria
- laparoscopic cholecystectomy patients
- indication for operation symptomatic gallstones
Exclusion criteria
- previous complication of gallstone disease
- indication for cholecystectomy other than symptomatic gallstones
- illness significantly lowering quality of life
- inability to fill in questionnaires
- denies participation
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Finland · 2 centers
- Jorvi, Helsinki University Hospital — Espoo
- HUS Hyvinkää Hospital — Hyvinkää
Identifiers
NCT: NCT03326154 · HUS/2317/2016