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Recruiting

NCT Number: NCT03326154

Post-Cholecystectomy Quality of Life

The study aims to identify factors associated with no increase in gastrointestinal quality of life after elective cholecystectomy for gallstones.

Recruiting

Interested in participating?

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Jorvi, Helsinki University Hospital, Espoo, Finland

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

No intervention, observational

Other

Observation

Primary outcomes

  1. Quality of life: Gastrointestinal Quality of Life GIQLI score

    Time frame: 1 year

    10 point improvement in Gastrointestinal Quality of Life GIQLI score

Study contacts

Contact information is provided by the study sponsor or research team.

Hanna Lampela, MD, PhD

CONTACT

[email protected]

+358504286224

Sponsors and collaborators

Lead sponsor

Helsinki University Central Hospital

Other

Registry information

Official study title

Health Related Quality of Life and Abdominal Symptoms After Cholecystectomy

Important dates

Study start
2017
Primary completion
2022
Study completion
2032
First posted
Oct 31, 2017
Registry last updated
Sep 3, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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