Actively Recruiting

Age: 18Years +
All Genders
ID03326154

Health Related Quality of Life and Abdominal Symptoms After Cholecystectomy

Led by Helsinki University Central Hospital · Updated on 2020-09-03

1000

Participants Needed

2

Research Sites

495 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to identify factors linked to no improvement in gastrointestinal quality of life after elective laparoscopic cholecystectomy for gallstones. The study focuses on patients who have symptomatic gallstones and undergo this surgery, with the goal of understanding outcomes related to abdominal symptoms and quality of life. Participants are observed without any additional intervention. The study monitors patients following their scheduled laparoscopic cholecystectomy, tracking their recovery and quality of life over time to gather data on gastrointestinal health. During the study, participants will complete questionnaires to assess their gastrointestinal quality of life using the GIQLI score at one year after surgery. Researchers will analyze these results to understand the impact of the surgery on abdominal symptoms and overall well-being. The study is observational and involves regular follow-up assessments over the course of the study period.

CONDITIONS

Brief Title

Post-Cholecystectomy Quality of Life

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who have undergone or are scheduled for laparoscopic cholecystectomy
  • Surgery indication is symptomatic gallstones
  • Adults aged 18 years or older
Not Eligible

You will not qualify if you...

  • Previous complications from gallstone disease
  • Surgery indication other than symptomatic gallstones
  • Illness that significantly lowers quality of life
  • Unable to complete questionnaires
  • Declines participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 1 year

Participants who have undergone or are scheduled for laparoscopic cholecystectomy are observed to assess their quality of life and abdominal symptoms over time.

Periodic visits to complete quality of life questionnaires

Trial Site Locations

Total: 2 locations

1

Jorvi, Helsinki University Hospital

Espoo, Finland

Actively Recruiting

2

HUS Hyvinkää Hospital

Hyvinkää, Finland

Actively Recruiting

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Research Team

H

Hanna Lampela, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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