Status:

NOT_YET_RECRUITING

RELIEF-pathway in Patients With Upper Abdominal Pain

Lead Sponsor:

Radboud University Medical Center

Conditions:

Abdominal Pain

Gallstone; Colic

Eligibility:

All Genders

18-70 years

Phase:

NA

Brief Summary

Upper abdominal pain (UAP) is a common symptom and frequently the reason to visit the hospital. The prevalence of epigastric pain in the Dutch population is estimated to be as high as 37%. Moreover, D...

Detailed Description

Objective: The main goal is to evaluate the effect of the RELIEF pathway versus usual care on health care utilization in terms of hospital visits and number of interventions. Study design: A multicen...

Eligibility Criteria

Inclusion

  • Patients between 18 and 70 years old.
  • First referral due to upper abdominal pain (UAP) and symptoms due to Functional dyspepsia (ICPC code 87.02), Irritable Bowel syndrome (ICPC 93.0) or uncomplicated symptomatic cholecystolithiasis (ICPC 98.03).
  • Proficient in reading and understanding of the Dutch language.
  • Referred to the outpatient clinic of gastroenterology or surgery.
  • Providing informed consent.

Exclusion

  • If the following alarm symptoms are reported in the referral letter by the GP: weight loss, persistent vomiting, dysphagia, jaundice, hematemesis, melena, haematochezia, or anaemia.
  • Any other direct or indirect signs of cancer or upper GI tract bleeding.
  • Patients with a first or second-degree relative with a history of upper GI tract malignant neoplasm.
  • Patients with a history of complicated cholecystolithiasis.
  • A history of or current malignancy (except SCC or BCC of the skin).
  • Pregnancy;
  • Expected short life span of less than 12 months.
  • Known cirrhosis of the liver
  • Current schizophrenia, memory deficiency, or any other disorder that predispose them to unreliable questionnaire responses;
  • Mentally incompetent;

Key Trial Info

Start Date :

May 1 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

May 1 2027

Estimated Enrollment :

471 Patients enrolled

Trial Details

Trial ID

NCT06002516

Start Date

May 1 2024

End Date

May 1 2027

Last Update

August 21 2023

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